Entries |
Document | Title | Date |
20080200974 | Drug Eluting Stent System with Controlled Self Expansion - A self-expanding stent providing a high compliance mismatch upon initial placement, to exert radially outward force over the course of several weeks or months until it reaches the limits of expansion as imposed by a limiting mechanism, and thereafter provide high resistance to inward radial forces exerted by the artery without exerting additional outward radial force on the artery. The stent is coated with a compound including an MMPI, in a formulation in which the MMPI is substantially exhausted over the course of several weeks or months, to be substantially coincident with expansion of the stent to its stop limited diameter. | 08-21-2008 |
20080228254 | Delivery systems and methods of implantation for replacement prosthetic heart valves - A method of delivering a replacement prosthetic valve to a previously implanted prosthetic valve including the steps of compressing a replacement prosthetic valve having an expandable stent within a sheath of a delivery system, wherein the delivery system comprises a proximal end, a distal end, and a centering structure positioned between the proximal and distal ends, advancing the delivery system and compressed replacement prosthetic valve into a vessel of a patient until the distal end of the delivery system is positioned adjacent to a second side of a previously implanted prosthetic valve, deploying the centering structure to radially reposition the distal end of the delivery system, further advancing the delivery system toward the previously implanted prosthetic valve, and deploying the replacement prosthetic valve | 09-18-2008 |
20080234794 | IMPLANTABLE STENTS HAVING A PLURALITY OF VARYING PARALLELOGRAMMIC CELLS AND METHODS FOR MANUFACTURING THE SAME - A stent for implantation within a body vessel is provided with a plurality of varying parallelogrammic cells. The stent is radially expandable from a compressed condition, suitable for inserting the device in an introducer, to a deployed or expanded condition within a body vessel. The stent includes a plurality of parallelogrammic body cells and a plurality of parallelogrammic flare cells. The flare cells have a substantially greater elongation ratio than the body cells. Also provided is a method for manufacturing stents having a plurality of varying parallelogrammic cells. | 09-25-2008 |
20080249597 | THIN FILM TISSUE REPAIR MATRIX - A tissue repair matrix has an intricate pattern of loops, struts and bridges and is made of a super elastic alloy. The repair matrix includes hooks which improve the ingrowth when implanted and amorphic circles which provide rounded surfaces to the outer edges which made the repair matrix a-traumatic when implanted. When the repair matrix is cooled the molecular phase becomes martensitic which allows the tissue repair matrix to be compressed for easier insertion into a patient. When the tissue repair matrix is heated, the molecular phase changes to austenitic which causes the tissue repair matrix to expand to a size suitable for medical procedure. | 10-09-2008 |
20080249598 | COVERED STENTS WITH DEGRADABLE BARBS - The present invention is directed at a removable stent for providing reinforcement to a selected region of a selected body lumen including a resilient cylindrical layer, including at least one bioresorbable extrusion exterior from the resilient cylindrical layer for resisting migration of the removable stent when the removable stent is positioned in the selected region of the selected body lumen. The present invention also includes a temporary implantable endoprosthesis which includes a tubular, radially compressible and axially flexible structure, including at least one bioresorbable extrusion exterior from the resilient cylindrical layer for resisting migration of the removable stent when the removable stent is positioned in the selected region of the selected body lumen. | 10-09-2008 |
20080255650 | METHODS AND APPARATUS FOR SURGICAL ANASTOMOSIS - Methods and apparatus for anastomosis of a lumen according to various aspects of the present invention operate in conjunction with an impermeable stent. The impermeable stent may comprise a scaffold and, if needed, a sealant, such as a membrane and/or adhesive. In one embodiment, the scaffold, membrane and/or adhesive comprise biocompatible materials suitable for bio-absorption and/or degradation. | 10-16-2008 |
20080262589 | Intravascular Implant - The invention has for its object the provision of an intravascular implant that has mechanical characteristics and physiological characteristics and is very low in cell cytotoxicity and provides an intravascular implant having an implant body made of a metal material that contains gadolinium and magnesium and is free of yttrium. | 10-23-2008 |
20080281393 | Bioabsorbable Self-Expanding Endolumenal Devices - The present invention is directed to bioabsorbable self-expanding medical devices for use inside or outside body conduits that self-expand at, or below, normal human body temperature without requisite for a polymeric thermal transition. | 11-13-2008 |
20080281394 | Covered stent having a dissolvable portion - An expandable stent having a covering which exhibits the characteristic of upon being activated by applying an agent to the covering, dissolving to expose a portion of the underlying stent. The stent may be placed across the neck of an aneurysm to seal the aneurysm, and thereafter a selected region of the covering may be dissolved by an activating agent to permit blood to flow to adjacent vessels. | 11-13-2008 |
20080300665 | MEDICAL IMPLANT, IN PARTICULAR STENT - A medical implantable stent comprising a main structure ( | 12-04-2008 |
20080312727 | Medical Implant Such a Stent - A medical implant such as a self-expanding shape memory alloy stent with a strut matrix formed by cut patterns in a wall of a tubular workpiece ( | 12-18-2008 |
20090005847 | Branched stent/graft and method of fabrication - Branched braided stent or graft devices and processes for fabrication of the devices are disclosed in which a trunk portion and two hinge leg portions are fabricated in one piece braided from a single plurality of filaments, whereby the legs contain the full plurality of filaments and the trunk portion contains a subset of the same plurality of filaments. The fabrication process involves braiding the hinged legs on a mandrel while retaining loops of filament between the hinged leg portions for subsequent braiding of the trunk portion of the stent or graft. | 01-01-2009 |
20090005848 | MODULAR VASCULAR PROSTHESIS AND METHODS OF USE - The present invention relates a vascular prosthesis and related assembly methods that includes a plurality of modular segments inter-engaged by flexible, and preferably lockable, inter-engageable elements forming joints or other connector areas. The segments may have a number of different mechanical properties and may be assembled by the clinician, through mechanical or chemical joining, to customize the prosthesis for a specific patient or application. | 01-01-2009 |
20090024198 | STENT WITH HELICAL ELEMENTS - An expandable stent comprised of a plurality of helical segments is disclosed. In one embodiment, the stent is generally cylindrical in shape having a cylindrical axis, and comprises a first and second set of helical segments. The helical segments in the first set are substantially parallel and have a first pitch forming a first helical angle with respect to the cylindrical axis. The helical segments in the second set are also generally parallel to each other and form a second pitch that differs from the first pitch, thereby forming a second helical angle with respect to the cylindrical axis. In an alternative embodiment, the stent comprises one set of helical segments and a plurality of circumferential elements that are joined together by the helical segments to form a plurality of cylindrical elements which are joined together to form a stent body. The stent may also have endzones. | 01-22-2009 |
20090030494 | Method and devices for treatment of vulnerable (unstable) and/or stable atherosclerotic plaque by disrupting pathologic vasa vasorum of the atherosclerotic plaque - A drug-eluting stent is disclosed; together with various methods for treating atherosclerotic plaques and other cardiovascular diseases via intervention on vasa vasorum. | 01-29-2009 |
20090036964 | Expandable Prostheses for Treating Atherosclerotic Lesions Including Vulnerable Plaques - The invention provides expandable tubular prostheses that are designed for the treatment of atherosclerotic lesions, such as vulnerable plaques, and that are characterized by no foreshortening, optimal radial force and accuracy of deployment. In the treatment of vulnerable plaque, the device may be expanded in a blood vessel so that its central section at least partially contacts a vulnerable plaque lesion and/or the blood vessel wall in close proximity to the vulnerable plaque lesion. The invention also provides more general methods of treating atherosclerosis and promoting endothelialization using the prostheses of the invention. | 02-05-2009 |
20090088828 | Electrically Charged Implantable Medical Device - A medical device comprises a tubular structure adapted for being implanted in the vasculature of a mammal, the tubular structure being formed, at least in part, of electrically charged nonwoven polymer fibers. | 04-02-2009 |
20090105797 | EXPANDABLE STENT - A stent includes a radially expandable tubular structure having a first end, a second end, and a primary strut arrangement extending over substantially an entire length thereof. The primary strut arrangement includes a plurality of rows of struts. The struts are interconnected within each row in a sinusoidal arrangement about a circumference of the tubular structure. Crests and troughs in the sinusoidal arrangement include connection points of the struts. A plurality of longitudinal struts connect neighboring rows of struts at the connection points. In each row, four circumferentially adjacent struts are disposed between every two longitudinal struts joined to the row. One of the two longitudinal struts extends in a direction of the first end to a first neighboring row, and the other of the two longitudinal struts extends in a direction of the second end to a second neighboring row. | 04-23-2009 |
20090149935 | EXPANDABLE STENT - An expandable stent designed to maintain a passageway through a body lumen of a patient is disclosed. The expandable stent is a tubular member that includes a thermoplastic material and woven or wound fibers at least partially in contact with the thermoplastic material, such that the thermoplastic material maintains the tubular member in at least one of an expanded state and a collapsed state. | 06-11-2009 |
20090157158 | Self-expanding biodegradable stent - The self-expanding biodegradable stent is a compressible, resilient mesh stent, which is compressed during delivery to a biological vessel or channel, and which expands to the contours of the vessel or channel upon delivery. The self-expanding biodegradable stent includes a substantially cylindrical main body portion having slightly flared, longitudinally opposed first and second open ends. The substantially cylindrical main body portion is hollow and is formed from an open mesh material, preferably formed as a unitary body from a biodegradable monofilament, such as a polydioxanone monofilament fiber. In order to reduce the possibility of trauma to the interior of the vessel, the open ends are blunted, with end points of the mesh forming a plurality of loops being about each of the first and second open ends, and opposing ends of the filament are interleaved with and bonded to a medial portion of the cylinder. | 06-18-2009 |
20090171426 | RADIALLY EXPANDABLE STENT - An expandable stent radially adjustable between a collapsed state and an expanded state. The stent generally includes a main body and a plurality of connector segments. The main body has first and second ends, a longitudinal axis extending from the first end to the second end, and a plurality of ring structures. Each of the plurality of connector segments joins adjacent ring structures. Some ring structures may be connected by a pair of diamond connector segments that define a diamond-shaped portion when the stent is in the expanded state. Some ring structures may be connected by flex connector segments oriented to permit rotation of the second ring structure about the longitudinal axis during radial expansion of the stent. | 07-02-2009 |
20090177259 | METHODS AND SYSTEMS FOR PLACEMENT OF A STENT ADJACENT AN OSTIUM - The present invention provides for treatment of ostial occlusions through placement of scaffold in a side-branch adjacent the ostium. | 07-09-2009 |
20090198315 | Vascular Stents, Methods of Use and Methods of Manufacture - Embodiments of the present invention are directed to medical implants/stents, systems, and methods of treatment using such stents. Some embodiments of the invention include a self-expanding stent having a tubular first wall structure of a first diameter, where each end portion of the first wall structure is formed into a second wall structure of a second diameter larger than the first diameter. A membrane covers at least the first wall structure and the stent includes an interlaced, helicoidally wound wire forming a mesh-like structure. | 08-06-2009 |
20090204196 | SELF-EXPANDABLE STENT WITH A CONSTRICTIVE COATING AND METHOD OF USE - The present invention provides a system and method for providing a coating on a self-expandable medical device, such as a stent, while avoiding the issues relating to coating damage from the delivery sheath during loading and deployment. In one embodiment, the present invention comprises a constrictive coating that acts as a constrictive sheath for the stent. A cutting mechanism is mounted on the end of the delivery tube such that when the stent with the constrictive coating exits the delivery tube, the constrictive coating is cut. This releases the constriction retaining the sheath, and the stent self-expands, pressing the cut portions of the coating against the lumen wall. | 08-13-2009 |
20090210045 | Stent - The invention relates to a stent for insertion into and placement inside a body cavity of a human being or an animal, said stent being intended for having a first configuration during insertion into the cavity and said stent, after having been placed in the cavity, being intended for having a second configuration. In an aspect of the invention, an expandable part is constituted by at least one first section of at least one helical winding in a clockwise direction and at least one second section of at least one helical winding in a counter-clockwise direction, each of said first and second at least one section being radially expandable so that during expansion, and where the at least one first section will be rotating in counter-clockwise direction and the at least one second section will be rotating in clockwise direction. In another aspect of the invention, a non-straight curvature of the retaining part is capable of conforming to a curvature of the body cavity, thereby avoiding migration of the stent along the body cavity, and substantially without application of radial forces from the retaining part onto the body cavity walls. | 08-20-2009 |
20090222075 | Method for Producing Strain Induced Austenite - This disclosure relates to shape memory alloys which have been subjected to a thermal and mechanical treatment to increase the austenite start temperature A | 09-03-2009 |
20090222076 | Self-Expandable Medical Instrument for Treating of Defects in a Patient's Heart - The invention relates to a self-expandable medical instrument ( | 09-03-2009 |
20090254164 | ENERGIZED STENTS AND METHODS OF USING THE SAME - The present disclosure relates to surgical systems including energized/energizable stents, and methods of using the same in the prevention of restenosis. A surgical system for treating a stenosis and/or a restenosis site s provided. The surgical system includes an electrosurgical generator; an energy transmitting conduit connectable to the electrosurgical generator; and a stent positionable in a body lumen at a site of a stenosis. The stent is fabricated from an electrically conductive material and adapted to electrically communicate with the electrosurgical generator, and the energy transmitting conduit delivers electrosurgical energy to the site of the stenosis. | 10-08-2009 |
20090264975 | MEDICAL DEVICES HAVING A COATING OF INORGANIC MATERIAL - In one aspect, a medical device has a first configuration and a second configuration, a reservoir containing a therapeutic agent, and a barrier layer disposed over the reservoir, wherein the barrier layer comprises an inorganic material. In another aspect, a medical device has a reservoir containing a therapeutic agent, a barrier layer disposed over the reservoir, wherein the barrier layer comprises an inorganic material, and a swellable material disposed between the barrier layer and a surface of the medical device, wherein the swellable material is a material that swells upon exposure to an aqueous environment. In yet another aspect, a medical device has a multi-layered coating having alternating reservoir layers and barrier layers, and a plurality of excavated regions penetrating through at least a partial thickness of the multi-layered coating. In yet another aspect, a medical device has a polymer layer comprising a block co-polymer, wherein the polymer layer contains a therapeutic agent, and a barrier layer disposed over the polymer layer, wherein the barrier layer comprises an inorganic material, and wherein the barrier layer has a plurality of discontinuities. Methods of forming coatings on medical devices and methods of delivering therapeutic agents to body sites are also disclosed. | 10-22-2009 |
20090287288 | METHODS AND APPARATUS FOR LUMINAL STENTING - Described herein are flexible implantable occluding devices that can, for example, navigate the tortuous vessels of the neurovasculature. The occluding devices can also conform to the shape of the tortuous vessels of the vasculature. In some embodiments, the occluding devices can direct blood flow within a vessel away from an aneurysm or limit blood flow to the aneurysm. Some embodiments describe methods and apparatus for adjusting, along a length of the device, the porosity of the occluding device. In some embodiments, the occluding devices allows adequate blood flow to be provided to adjacent structures such that those structures, whether they are branch vessels or oxygen-demanding tissues, are not deprived of the necessary blood flow. | 11-19-2009 |
20090299448 | ANEURYSM TREATMENT SYSTEM - An aneurysm treatment system includes a sleeve with a breach or a breachable facet disposed therein. The facet allows a guide structure to breach the sleeve and to deliver a portion of the sleeve continuously to an aneurysm. | 12-03-2009 |
20100004725 | HELICAL IMPLANT HAVING DIFFERENT ENDS - Preferred embodiments of an implantable medical device with a high degree of flexibility is shown and described. One aspect includes an implantable stent having an intermediate portion with a helical winding and first and second end portions. The implantable stent further includes a coupling portion with a helical winding, and bridges joining struts of defining the helical windings. The stent also includes a paddle providing a bridge joining the ends or the helical windings. Another aspect relates to a radially self-expansible stent with a plurality of radiopaque markers attached to it. The markers are shaped and located at the stent end such that the compressive stress exerted on the end annulus of the stent during release of the stent is shared between the markers and the inflection zones that do not carry a marker. | 01-07-2010 |
20100004726 | SELF-EXPANDING PSEUDO-BRAIDED INTRAVASCULAR DEVICE - A self-expanding, pseudo-braided device embodying a high expansion ratio and flexibility as well as comformability and improved radial force. The pseudo-braided device is particularly suited for advancement through and deployment within highly tortuous and very distal vasculature. Various forms of the pseudo-braided device are adapted for the repair of aneurysms and stenoses as well as for use in thrombectomies and embolic protection therapy. | 01-07-2010 |
20100004727 | SYSTEM FOR IMPLANTING A VALVE PROSTHESIS - A valve prosthesis ( | 01-07-2010 |
20100023105 | VASCULAR REMODELING DEVICE - A generally spherical vascular remodeling device is permanently positionable at a junction of afferent and efferent vessels of a bifurcation having an aneurysm. After positioning the device at the junction to substantially conform the device to the shape of the junction, the device acts as a scaffolding to inhibit herniation of objects out of the aneurysm and the device permits perfusion to the efferent vessels. Positioning the device may include deployment and mechanical or electrolytic release from a catheter. Embolic material may be inserted in the aneurysm before or after positioning the device. The device may have a first end, a second end substantially opposite to the first end, and a plurality of filaments extending between and coupled at the first end and the second end. Such devices may be football shaped, pumpkin shaped, or twisted. The device may include a plurality of loops forming a generally spherical shape. | 01-28-2010 |
20100049291 | STENT WITH IMPROVED RESISTANCE TO MIGRATION - A modular mating stent is adapted to resist migration within a receiving stent. The modular mating stent has a substantially self-expandable first section of predetermined compressibility that is adapted to permit the first section to conform to the shape of a body lumen surrounding the first section. The modular mating stent also has a balloon-expandable second section that is less compressible than the first section, which is adapted to firmly engage a surface of the receiving stent surrounding the second section. | 02-25-2010 |
20100094389 | SELF-EXPANDABLE STENT SYSTEMS FOR BIFURCATED LESIONS - Self-expandable bifurcation stent and systems for delivery and implantation of the self-expandable bifurcation stent, comprising a self-expandable bifurcation stent made of a material possessing shape memory, capable of shaping a mesh with cylindrical surface and marked by radioactive labels, and the delivery system for its implantation, comprising a polymeric tubular catheter with a cap at the distal end, a guiding wire and a pushing wire, where the tubular catheter is executed double-barreled, one lumen accommodating the guiding wire, and the second lumen accommodating the pushing wire with a cap at its distal end, which cap is executed in the shape of a polymeric elastic cap put over the tubular catheter accommodating, between the polymeric elastic cap and the tubular catheter, the stent in the first position with the reduced diameter, the cap is executed with the capability of distal | 04-15-2010 |
20100100166 | LONGITUDINALLY FLEXIBLE STENT - An intravascular stent especially suited for implanting in curved arterial portions. The stent retains longitudinal flexibility after expansion. The stent is formed of intertwined meander patterns forming triangular cells. The triangular cells are adapted to provide radial support, and also to provide longitudinal flexibility after expansion. The triangular cells provide increased coverage of a vessel wall. The stent can have different portions adapted to optimize radial support or to optimize longitudinal flexibility. Loops in the stent are disposed and adapted to cooperate so that after expansion of said stent within a curved lumen, the stent is curved and cells on the outside of the curve open in length, but narrow in width whereas cells on the inside of the curve shorten in length but thicken in width to maintain a density of stent element area which much more constant than otherwise between the inside and the outside of the curve. As a result, when the stent is coated with a medicine the more constant density of stent elements results in an even dose being applied to the inside wall of the lumen, avoiding the possibility that a toxic dose be supplied at one area while a less than effective dose is applied to another area. | 04-22-2010 |
20100121423 | Stent with Vessel Valve - The invention relates to a stent that comprises a single sinus section and is preferably provided at the proximal end thereof with a native vessel valve ( | 05-13-2010 |
20100131037 | RADIOPAQUE POLYMERIC STENTS - The present invention relates to polymeric medical devices such as stents. More particularly the polymeric compositions disclosed herein comprise halogen-containing, tyrosine-derived diphenols, optionally in conjunction with other groups, such as dicarboxylic acids and/or poly(alkylene oxides), such that the medical devices made from these polymeric compositions are bioresorbable and inherently radiopaque, and exhibit physicomechanical properties consistent with the intended uses of such devices. | 05-27-2010 |
20100211152 | STENT HAVING HELICAL ELEMENTS - An expandable stent comprised of a plurality of helical segments is disclosed. In one embodiment, the stent is generally cylindrical in shape having a cylindrical axis, and comprises a first and second set of helical segments. The helical segments in the first set are substantially parallel and have a first pitch forming a first helical angle with respect to the cylindrical axis. The helical segments in the second set are also generally parallel to each other and form a second pitch that differs from the first pitch, thereby forming a second helical angle with respect to the cylindrical axis. In an alternative embodiment, the stent comprises one set of helical segments and a plurality of circumferential elements that are joined together by the helical segments to form a plurality of cylindrical elements which are joined together to form a stent body. The stent may also have endzones. | 08-19-2010 |
20100262216 | Stent having a C-shaped body section for use in a bifurcation - A bifurcation stent system includes a pair of self-expanding stents. Each stent has a C-shaped body section having a generally semicircular cross-section along its length and an O-shaped body section having a circular cross-section along its length. The stents are deployed in vivo such that the edges of the C-shaped body sections abut each other to form a tubular scaffold in a Y-shaped formation that conforms to the bifurcation. In order to connect the stents in vivo, the C-shaped body sections are configured to include a ball and socket connection there between. The C-shaped body sections align and abut to form a tubular scaffold that extends in the main vessel of the bifurcation, while the O-shaped body sections are tubular scaffolds that extend into the respective branch legs of the bifurcation. | 10-14-2010 |
20100280586 | MEDICAL DEVICE WITH TENSIONABLY ATTACHED REMODELABLE MATERIAL - Medical devices for implantation in a body vessel, and methods of using and making the same, are provided. A medical device includes a support frame having struts and a weakened frame portion, and a remodelable material tensionably attached to the support frame. The weakened frame portion has a first configuration in which the support frame has a first outward radial force and a second configuration in which the support frame has a second, lesser outward radial force. The remodellable material restricts expansion of the frame from a radially compressed configuration to a radially expanded configuration when the weakened frame portion is in the first configuration. The remodelable material can form one or more valve leaflets adapted to regulate fluid flow in a body vessel, such as a vein. | 11-04-2010 |
20100280587 | VARIABLE DENSITY BRAID STENT - A stent comprises at least one stent member woven to form a substantially tubular body that defines a flow path. The tubular body comprises a first region and a second region. In the first region the at least one stent member defines a plurality of first region openings and in the second region at least one first portion of the at least one member and at least one second portion of the at least one member are engaged together to form at least one primary strand. The at least one primary strand defines a plurality of second region openings. The at least one of the plurality of second region openings is in fluid communication with the flow path. The plurality of second region openings provide the second region with a greater porosity than the first region. | 11-04-2010 |
20100298921 | BEND-CAPABLE TUBULAR PROSTHESIS - Stent exhibiting a succession of turns around the axis, adjacent turns being connected by connector portions distributed around the circumference of the prosthesis, each of the turns being made up of struts that extend the length of the turn and are interspersed by inflection zones located at the axial ends of each of the turns. When the prosthesis expands radially, gaps open up between adjacent struts of each of the turns, the inflection zones being distributed regularly around the circumference so that the gaps are substantially the same size as each other around the circumference of the turn, characterised in that at least every second turn exhibits a stagger zone within which the said gap between adjacent said struts is of an individual size different from that common to the other gaps of that second turn. | 11-25-2010 |
20100331946 | SHAPE MEMORY ALLOY ARTICLES WITH IMPROVED FATIGUE PERFORMANCE AND METHODS THEREFORE - Articles made of shape memory alloys having improved fatigue performance and to methods of treating articles formed from shape memory alloy materials by pre-straining the articles (or desired portions of the articles) in a controlled manner so that the resultant articles exhibit improved fatigue performance. The shape memory articles are preferably medical devices, more preferably implantable medical devices. They are most preferably devices of nitinol shape memory alloy, most particularly that is superelastic at normal body temperature. The pre-straining method of the present invention as performed on such articles includes the controlled introduction of non-recoverable tensile strains greater than about 0.20% at the surface of a desired portion of a shape memory alloy article. Controlled pre-straining operations are performed on the shape-set nitinol metal to achieve non-recoverable tensile strain greater than about 0.20% at or near the surface of selected regions in the nitinol metal article. The pre-straining operations result in a significant increase in fatigue life of the selectively treated regions and an overall improvement in the fatigue performance of the device. | 12-30-2010 |
20110015716 | TUBE WITH REVERSE NECKING PROPERTIES - An improved tubular structure adapted to increase in diameter upon application of axial force is provided. Increase in diameter is achieved by constructing the tube from multiple layers of material that move relative to each other during axial elongation of the tube. The tube of the present invention can be used both to avoid problems in “necking” found in many prior tube devices, and to provide additional benefits that increases in diameter of the tube during axial elongation can provide. As such, the tube of the present invention may be useful as a manufacturing aid, as a deployment sheath (for example, to deliver medical devices), and in other applications that may benefit from easier tubular sheath removal. | 01-20-2011 |
20110029059 | Prosthesis Coupling Device and Method - A coupling device ( | 02-03-2011 |
20110066220 | APPARATUS AND METHODS FOR CONDUITS AND MATERIALS - The present invention provides apparatus and methods for a conduit, such as an implantable conduit for a vessel. The conduit may comprise a main member and a side-branch member. The conduit may be implanted with the side-branch member initially disposed within the main member. When positioned, the side-branch member may then be extended from within the main member and into a vessel side-branch. The materials for the conduit may include circumferentially distensible and/or low recoil materials. The materials for the conduit may be constructed by various techniques and may include materials with enhanced flexibility and kink resistance. | 03-17-2011 |
20110071612 | ANTI-ANGIOGENIC COMPOSITIONS AND METHODS OF USE - The present invention provides compositions comprising an anti-angiogenic factor, and a polymeric carrier. Representative examples of anti-angiogenic factors include Anti-Invasive Factor, Retinoic acids and derivatives thereof, and taxol. Also provided are methods for embolizing blood vessels, and eliminating biliary, urethral, esophageal, and tracheal/bronchial obstructions. | 03-24-2011 |
20110082533 | Extendible Stent Apparatus - A stent apparatus with at least one side opening which may further comprise an extendable stent portion laterally extending from the side opening and at least partly in registry with the wall of the side opening. Devices constructed in accordance with the invention include, singularly or in combination, a main expandable stent comprising at least one substantially circular side opening located between its proximal and distal end openings, which side opening may further comprise an expandable portion extending radially outward from the edges of the side opening; and a branch stent comprising proximal and distal end openings and which may further comprise a contacting portion at its proximal end, and which may optionally be constructed to form either a perpendicular branch or a non-perpendicular branch when inserted through a side opening of the main stent. | 04-07-2011 |
20110125243 | STENT HAVING AN EXPANDABLE WEB STRUCTURE - A stent comprises a tubular flexible body composed of a web structure that is expandable from a contracted delivery configuration to a deployed configuration and that comprises neighboring web patterns of alternating concavities extending circumferentially and adjoined by X-shaped transition sections. The web pattern may comprise either arcuate struts interconnected by bends, or a plurality of substantially straight sections with the transition sections formed by the junctions between pairs of adjacent bends of opposite curvatures. | 05-26-2011 |
20110130819 | MODULAR ENDOGRAFT DEVICES AND ASSOCIATED SYSTEMS AND METHODS - Modular endograft devices and associated systems and methods are disclosed herein. In several embodiments, an endograft system can include a first endograft device and a second endograft device that each include an integrated frame, a cover and a lumen within the cover. Each endograft device further includes a superior portion and an inferior portion. The superior portion can have a convexly curved outer wall and a septal wall. The first and second endograft devices can be configured to extend into a low-profile configuration with a first cross-sectional dimension and a first length and self-expand into an expanded configuration with a second cross-sectional dimension greater than the first cross-sectional dimension and a second length less than the first length. In the expanded configuration, the septal walls can press against each other and form a septum between the lumens of the first and second endograft devices. | 06-02-2011 |
20110152993 | MULTIPLE LAYER FILAMENTARY DEVICES OR TREATMENT OF VASCULAR DEFECTS - Devices and methods for treatment of a patient's vasculature with some embodiments configured for delivery with a microcatheter for treatment of the cerebral vasculature of a patient. Some embodiments may include a permeable shell and inner structure configured to occlude blood flow therethrough. | 06-23-2011 |
20110172753 | ENDOPROSTHESES - Endoprosthesis are disclosed. | 07-14-2011 |
20110202122 | STENT - A stent includes a stent body in which struts are joined mutually while intersecting and which is formed tubularly as a whole, and a drug coat layer on the outer surface of the struts. The strut has a bend which is deformed as the stent body expands/contracts in the radial direction, and the drug coat layer with which the bend is coated is formed in such a manner that the drug coat layer is mountain-shaped in a cross-section perpendicular to the axis of the strut and the ridgeline of the mountain shape extends in a wavy shape along the longitudinal direction of the strut. The drug coat layer deforms relatively easily without using plasticizer as the stent deforms and is not so susceptible to causing problems such as peeling, destruction, damage or falling off of the drug coat later | 08-18-2011 |
20110224770 | Drug Eluting Stents and Methods of Making the Same - A stent formed from a bioabsorbable polymer matrix including at least one bioabsorbable polymer and at least one therapeutic agent dispersed therein, and methods of making the same. | 09-15-2011 |
20110288621 | PROSTHETIC VALVE WITH EXTERNAL SUPPORT FRAME - Prosthetic valves, methods of making medical devices, and methods of treatment are provided. The prosthetic valves of the invention have a valve portion moveable between first and second positions, and a spacing member that has a thickness and protects a portion of the valve portion from contact with a wall of a vessel in which the prosthetic valve is implanted, and/or another structural component of the prosthetic valve, such as a support frame. | 11-24-2011 |
20110313502 | COMPOSITE VASCULAR PROSTHESIS - A novel treatment for atherosclerotic vascular disease is described utilizing the implantation of a thin, conformable biocompatible prosthesis constructed from a composite of various structural and therapeutic scaffolds in combination with one or more bioactive agents. This prosthesis can be delivered into position over a lesion in order to passivate atherosclerotic plaques with minimal remodeling of the artery, or alternatively can be applied with a balloon to passivate the remodeled site. The composite prosthesis itself provides mild structural reinforcement of the vessel wall and an evenly distributed platform for the introduction of bioactive therapeutic agents. | 12-22-2011 |
20120010690 | METHOD AND APPARATUS FOR STENTING - A method and apparatus to create a more favorable flow regime in a lumen. An artificial shape in the lumen is created to at least one of eliminate flow disturbances and enchance aspects of fluid flow through a treatment site. | 01-12-2012 |
20120046726 | AORTIC VALVE STENT GRAFT - An implantable endoluminal prosthesis for replacing a damaged aortic valve is provided. In one embodiment, the prosthesis includes a balloon-expandable stent, a tubular conduit that extends into the ascending aorta, and a self-expanding stent. The tubular conduit extends across the balloon-expandable stent. The tubular conduit includes an artificial valve. The self-expanding stent extends across the tubular conduit into the ascending aorta. The balloon-expandable stent, the tubular conduit, and the self-expanding stent are coupled to provide unidirectional flow of fluid into the aorta and further into the coronary arteries. Also provided is a method for implanting the endoluminal prosthesis. | 02-23-2012 |
20120046727 | INTRALUMINAL STENT GRAFT - A method of making an tubular intraluminal graft in the form of a tubular diametrically adjustable stent having a tubular covering of porous expanded polytetrafluoroethylene which is less than 0.10 mm thick. The covering may be on the exterior surface of the stent, or on the interior surface of the stent, or both. The covering may be affixed to the stent by an adhesive which is preferably fluorinated ethylene propylene. | 02-23-2012 |
20120130467 | INTERFACIAL STENT AND METHOD OF MAINTAINING PATENCY OF SURGICAL FENESTRATIONS - A method according to one embodiment for maintaining patency of an opening inside the human body comprises introducing a radially self-expanding hollow stent into the opening while the stent is retained in a radially compressed state, wherein the stent has enlarged ends and a reduced intermediate portion. The stent is introduced into the opening such that its intermediate portion extends through the opening and the enlarged ends are positioned outside of the opening. Once deployed, at least the end portions of the stent expand on opposing faces of the opening to resist dislodgement of the stent from the opening. The stent is preferably biodegradable, such that it is eliminated from the surgical site over a period of weeks to months, by which time the patency of the opening is more assured. The method can be used in combination with, for example, an endoscopic surgical method such as endoscopic third ventriculostomy for treating hydrocephalus of a brain. | 05-24-2012 |
20120143300 | MEDICAL IMPLANT - Disclosed is a self-expanding medical implant for placement within a lumen of a patient. The implant comprises a woven or non-woven structure having a substantially tubular configuration, and is designed to be low-profile such that it is deliverable with a small diameter catheter. The implant has a high recoverability and desired mechanical properties. | 06-07-2012 |
20120271396 | BIODEGRADABLE ENDOPROSTHESES AND METHODS FOR THEIR FABRICATION - The disclosure provides biodegradable implantable devices such as a stent comprising a biodegradable polymeric wherein the polymeric material is treated to control crystallinity and/or Tg. The stent is capable to expand at body temperature from a crimped configuration to a deployed diameter and have sufficient strength to support a body lumen. | 10-25-2012 |
20120283811 | BIODEGRADABLE, BIOABSORBABLE STENT ANCHORS - Biodegradable/bioabsorbable stent anchors are provided to prevent stent migration and permit repositioning and/or removal of the stent after the anchors or portion thereof has sufficiently degraded or been absorbed. | 11-08-2012 |
20120290062 | INTRA-ATRIAL IMPLANTS MADE OF NON-BRAIDED MATERIAL - Several unique intra-cardiac pressure devices, placement catheters, methods of placement and methods of treating heart failure are presented. The intra-cardiac pressure devices presented allow sufficient flow from the left atrium to the right atrium to enable the relief of elevated left atrial pressure and resulting patient symptoms. The intra-cardiac pressure devices are made of a non-braided material. | 11-15-2012 |
20120316632 | Retrievable covered stent for bifurcation aneurysms - A retrievable covered stent has a self-expandable covered stent on the distal end and is particularly useful for occluding the neck of an aneurysm located in the vicinity of bifurcations or trifurcations of vessels. The said retrievable covered stent comprises a proximal retrieving structure and a proximal self-expandable supporting stent for supporting and retaining a smaller self-expandable covered stent on the distal end which is used to seal the neck of a bifurcation aneurysm. | 12-13-2012 |
20120323298 | SHAPE MEMORY ALLOY ARTICLES WITH IMPROVED FATIGUE PERFORMANCE AND METHODS THEREFORE - Articles made of shape memory alloys having improved fatigue performance and to methods of treating articles formed from shape memory alloy materials by pre-straining the articles (or desired portions of the articles) in a controlled manner so that the resultant articles exhibit improved fatigue performance. The shape memory articles are preferably medical devices, more preferably implantable medical devices. They are most preferably devices of nitinol shape memory alloy, most particularly that is superelastic at normal body temperature. The pre-straining method of the present invention as performed on such articles includes the controlled introduction of non-recoverable tensile strains greater than about 0.20% at the surface of a desired portion of a shape memory alloy article. Controlled pre-straining operations are performed on the shape-set nitinol metal to achieve non-recoverable tensile strain greater than about 0.20% at or near the surface of selected regions in the nitinol metal article. | 12-20-2012 |
20130041450 | ENDOPROSTHESIS FOR VASCULAR BIFURCATION - An apparatus for treating an area of bifurcation where a principal body conduit separates into at least two secondary conduits comprises a radially expandable first stent body. The first stent body has a substantially conical shape and a first end having a greater diameter than a second end when fully expanded. The first stent body is preferably shaped to be independent of any other stent bodies, and is free of any means for connecting to any other stent bodies when fully expanded. | 02-14-2013 |
20130073023 | Stent - A stent insertable in a body vessel, the body vessel defining a vessel wall. The stent includes a plurality of struts, the struts defining a substantially elongated stent passageway, the struts being configured, sized and operatively coupled to each other in a manner such that the stent is deformable between a first configuration and a second configuration. In the first configuration, the stent passageway has a first radial dimension and a first longitudinal dimension, and in the second configuration, the stent has a second radial dimension and a second longitudinal dimension, the second radial dimension being at least as large as the first radial dimension and the second longitudinal dimension being larger than the first longitudinal dimension. The stent is able to expand substantially longitudinally with the body vessel as the body vessel grows without reducing in diameter so as to reduce risks of damaging the vessel wall as the body vessel grows. | 03-21-2013 |
20130090713 | RADIALLY EXPANDABLE STENT - The invention relates to a radially expandable vessel support ( | 04-11-2013 |
20130110221 | Stent with Inwardly-Directed Protrusion | 05-02-2013 |
20130116768 | Composite Medical Textile Material and Implantable Devices Made Therefrom - An implantable composite medical device having a longitudinal length a woven textile portion having yarns interlaced in a woven pattern, a knitted textile portion having yarns interlooped in a knitted pattern. The woven and knitted portions are securably attached to one and the other to provide a composite woven and knitted textile surface along the longitudinal length of the device. The woven portion may have a permeability from about 30 to about 500 ml/min/cm | 05-09-2013 |
20130150943 | BIODEGRADABLE ENDOPROSTHESES AND METHODS FOR THEIR FABRICATION - The disclosure provides biodegradable implantable devices such as a stent comprising a biodegradable polymeric wherein the polymeric material is treated to control crystallinity and/or Tg. The stent is capable to expand at body temperature from a crimped configuration to a deployed diameter and have sufficient strength to support a body lumen. | 06-13-2013 |
20130166010 | HYBRID BALLOON-EXPANDABLE/SELF-EXPANDING PROSTHESIS FOR DEPLOYMENT IN A BODY VESSEL AND METHOD OF MAKING - A hybrid prosthesis for deployment in a body vessel includes a tubular stent body comprising a wire comprising a shape memory alloy, where the tubular stent body has a self-expanding portion comprising a distal portion of the wire and a balloon-expandable portion comprising a proximal portion of the wire. The shape memory alloy comprises an A | 06-27-2013 |
20130197617 | STENT - The invention relates to a medical device and a method of using it. The device is a stent which can be percutaneously deliverable with (or on) an endovascular catheter or via other surgical or other techniques and then expanded. The stent is configured to have a central portion defined by “open” cells and at least two end portions, defined by “closed” cells, spaced apart and directly connected to the distal and proximal ends of the central portion of the stent. The stent may also optionally have a covering or a lattice with openings. | 08-01-2013 |
20130211489 | Methods, Systems and Devices for Treatment of Cerebrospinal Venous Insufficiency and Multiple Sclerosis - Methods and devices for relieving stenoses in, or otherwise improving blood flow through, body lumens. Although applicable in a variety of different body lumens, the methods and devices of this invention are specifically useable for relieving stenoses in, or otherwise improving blood flow through, veins which drain blood from the brain for treatment of multiple sclerosis or other neurodegenerative disorders that are caused, triggered or exacerbated by venous occlusion or venous insufficiency. | 08-15-2013 |
20130218253 | SCAFFOLD SYSTEM FOR TISSUE REPAIR - A device for treating a damaged tissue includes an expandable scaffold positionable in a portion of a luminal tissue structure of a mammal; and maintained via stent technology, wherein the scaffold is comprised of electrospun fibers composed of a biodegradable compound. The scaffold serves as a temporary template that allows the tissue to be rebuilt. | 08-22-2013 |
20130218254 | MEDICAL DEVICE - A medical device with a radially compressible and expandable lattice structure ( | 08-22-2013 |
20130268044 | DURABLE STENT GRAFT WITH TAPERED STRUTS AND STABLE DELIVERY METHODS AND DEVICES - Some embodiments relate in part to endovascular prostheses and methods of deploying same. Embodiments may be directed more specifically to stent grafts and methods of making and deploying same within the body of a patient. Stent embodiments may include tapered struts for an even distribution of strain. Stent embodiments may also include portions which are enlarged in a circumferential direction which may be configured to stabilize the stent in a constrained state. | 10-10-2013 |
20130274849 | STENTS HAVING RADIOPAQUE MESH - A stent including a mesh made of strands. The mesh has at least one radiopaque strand and at least one non-radiopaque strand, and the at least one radiopaque strand and the at least one non-radiopaque strand each have different diameters. Each strand has an index of wire stiffness EI, where EI is the mathematical product of the Young's modulus (E) and the second moment of area (I). The EI of all strands in the mesh is no more than five times the EI of the strand having the smallest EI of any of the strands. | 10-17-2013 |
20130289690 | PERSONALIZED PROSTHESIS AND METHODS OF USE - A personalized prosthesis for implantation at a treatment site of a patient includes a self-expanding mesh or membrane having collapsed and expanded configurations. The collapsed configuration is adapted to be delivered to the treatment site, and the expanded configuration engages the personalized prosthesis with the treatment site. The mesh or membrane is personalized to match the treatment site in the expanded configuration, and has an outer surface that substantially matches the treatment site shape and size. The self-expanding mesh or membrane forms a central lumen configured to allow blood or other body fluids to flow therethrough. Methods of manufacturing and delivery of the personalized prosthesis are also disclosed. | 10-31-2013 |
20130304177 | Drug Eluting Medical Implant - Disclosed are self-expanding medical implants for placement within a lumen of a patient. The implants comprise a woven or non-woven structure having a substantially tubular configuration, and are designed to be low-profile such that they are deliverable with a small diameter catheter. The implants have a high recoverability and desired mechanical properties. | 11-14-2013 |
20130317589 | RETRIEVAL SYSTEMS AND METHODS FOR USE THEREOF - The devices and methods described herein relate to improved structures for removing obstructions from body lumens. Such devices have applicability in through-out the body, including clearing of blockages within the vasculature, by addressing the frictional resistance on the obstruction prior to attempting to translate and/or mobilize the obstruction within the body lumen. | 11-28-2013 |
20130338751 | METHOD OF TREATING VASCULAR BIFURCATIONS - A prosthesis is disclosed for placement across an ostium opening from a main body lumen to a branch body lumen. The prosthesis comprises a radially expansible support at one end, a circumferentially extending link at the other end and at least one frond extending axially therebetween. The circumferential link can comprise a catheter securement portion and a frond engagement portion. | 12-19-2013 |
20130345785 | FENESTRATED STENT GRAFTS - A stent graft ( | 12-26-2013 |
20140052230 | IMPLANTS HAVING HIGH FATIGUE RESISTANCE, IMPLANT DELIVERY SYSTEMS, AND METHODS OF USE - According to one aspect of the present invention, a fatigue resistant stent includes a flexible tubular structure having an inside diameter, an outside diameter, and a sidewall therebetween and having apertures extending through the sidewall. According to other aspects of the invention, processes for making a fatigue resistant stent are disclosed. According to further aspects of the invention, delivery systems for a fatigue resistant stent and methods of use are provided | 02-20-2014 |
20140100644 | DRUG-ELUTING MEDICAL IMPLANTS - Disclosed are self-expanding medical implants for placement within a lumen of a patient. The implants comprise a woven or non-woven structure having a substantially tubular configuration, and are designed to be low-profile such that they are deliverable with a small diameter catheter. The implants have a high recoverability and desired mechanical properties. | 04-10-2014 |
20140114389 | PLAIN WOVEN STENTS - Self-expandable, woven intravascular devices for use as stents (both straight and tapered), filters (both temporary and permanent) and occluders for insertion and implantation into a variety of anatomical structures. The devices may be formed from shape memory metals such as nitinol. The devices may also be formed from biodegradable materials. Delivery systems for the devices include two hollow tubes that operate coaxially. A device is secured to the tubes prior to the implantation and delivery of the device by securing one end of the device to the outside of the inner tube and by securing the other end of the device to the outside of the outer tube. The stents may be partially or completely covered by graft materials, but may also be bare. The devices may be formed from a single wire. The devices may be formed by either hand or machine weaving. The devices may be created by bending shape memory wires around tabs projecting from a template, and weaving the ends of the wires to create the body of the device such that the wires cross each other to form a plurality of angles, at least one of the angles being obtuse. The value of the obtuse angle may be increased by axially compressing the body. | 04-24-2014 |
20140128957 | SHAPED OCCLUDING DEVICES AND METHODS OF USING THE SAME - A self-expanding stent includes a proximal portion having a first cross-sectional area in an expanded state, a distal portion having a second cross-sectional area in an expanded state, a narrowed portion between the proximal portion and the distal portion, the narrowed portion comprising a cross-sectional area when in an expanded state that is less than the first cross-sectional area and the second cross-sectional area, wherein the narrowed portion is configured to increases flow velocity in the narrowed portion while reducing reduce pressure against a distal wall of the aneurysm by being axially disposed substantially between a proximal edge and a distal edge of an aneurysm neck or ostium, the flow traversing through the lumen of the self-expanding stent. In use, the self-expanding stent is positioned at the site of an aneurysm and expanded via release from a stent delivery device. | 05-08-2014 |
20140135888 | STENTS HAVING A HYBRID PATTERN AND METHODS OF MANUFACTURE - An intravascular stent have a hybrid pattern is disclosed herein. | 05-15-2014 |
20140148888 | STENT GRAFT HAVING A CLOSEABLE FENESTRATION - A radially expandable stent graft | 05-29-2014 |
20140194967 | DEVICE AND METHOD FOR TACKING PLAQUE TO BLOOD VESSEL WALL - A tack device for holding plaque against blood vessel walls in treating atherosclerotic occlusive disease can be formed as a thin, annular band of durable, flexible material. The tack device may also have a plurality of barbs or anchoring points on its outer annular periphery. The annular band can have a length in the axial direction of the blood vessel walls that is about equal to or less than its diameter as installed in the blood vessel. A preferred method is to perform angioplasty with a drug eluting balloon as a first step, and if there is any dissection to the blood vessel caused by the balloon angioplasty, one or more tack devices may be installed to tack down the dissected area of the blood vessel surface. | 07-10-2014 |
20140277329 | SECURED STRAND END DEVICES - A woven, self-expanding stent device has one or more strands and is configured for insertion into an anatomical structure. The device includes a coupling structure secured to two different strand end portions that are substantially aligned with each other. The two different strand end portions include nickel and titanium. The coupling structure is not a strand of the device. | 09-18-2014 |
20140296956 | GRADUALLY SELF-EXPANDING STENT - A gradually self-expanding stent is provided with a first region of stent cells. A restraining material is attached to the first region and restrains the first region from expanding to the expanded configuration. Over time the restraining material releases the first region to allow the first region to expand to the expanded diameter. The first region is located longitudinally between two second regions. The second regions expand at a faster rate than the first region. | 10-02-2014 |
20140296957 | GRADUALLY SELF-EXPANDING STENT - A gradually self-expanding stent is provided with a plurality of stent cells. A restraining material is attached to the stent structure and restrains the stent structure from expanding to the expanded configuration. Over time the restraining material releases the stent structure to allow the stent structure to expand to the expanded diameter. An anti-thrombotic drug is incorporated into the restraining material. | 10-02-2014 |
20140371836 | EXPANDABLE SUPPORTIVE ENDOLUMINAL STENT GRAFT - An endoluminal prosthesis having a graft sleeve, a set of internal graft channels formed within the graft sleeve and a self-expanding wire stent. The graft sleeve forms a main fluid flow channel between a first open end and a second open end of the graft sleeve and includes an external surface and an internal surface. The self-expanding wire stent is coaxially mounted with the graft sleeve and affixed to the graft sleeve. The set of internal graft channels includes at least two internal graft channels parallel to the graft sleeve, each internal graft channel having an inner open end within the first open end of the graft sleeve and an outer open end within the second open end of the graft sleeve, thereby forming a set of fluid flow channels between the end openings of the graft sleeve. | 12-18-2014 |
20140379063 | STENT - A stent and method of exhibiting radiopaque properties in a stent are disclosed, which includes a stent main body that is made of a metal, and a radiopaque marker that is made of a complete solid solution alloy having a corrosion potential of +200 mV of a corrosion potential of the metal of the stent main body. | 12-25-2014 |
20150039072 | FLEXIBLE STENT - The stent of the present invention combines a helical strut band interconnected by coil elements. This structure provides a combination of attributes that are desirable in a stent, such as, for example, substantial flexibility, stability in supporting a vessel lumen, cell size and radial strength. The structure of the stent of the present invention provides a predetermined geometric relationship between the helical strut band and interconnected coil elements in order to maintain connectivity at any diameter size state of the stent. | 02-05-2015 |
20150080999 | SELF-EXPANDING STENT - A self-expanding stent ( | 03-19-2015 |
20150081000 | BRAIDED SCAFFOLDS - A braided polymeric scaffold, made at least in part from a bioresorbable material is deployed on a catheter that uses a push-pull mechanism to deploy the scaffold. A drug coating is disposed on the scaffold. A plurality of scaffold segments on a catheter is also disclosed. | 03-19-2015 |
20150148882 | ANTI-THROMBOGENIC MEDICAL DEVICES AND METHODS - Methods for applying layers to medical devices and related devices are provided. Such devices can include stents. For example, the device can include a sidewall and a plurality of pores in the sidewall that are sized to inhibit flow of blood through the sidewall into an aneurysm to a degree sufficient to lead to thrombosis and healing of the aneurysm when the tubular member is positioned in a blood vessel and adjacent to the aneurysm. The device can have an anti-thrombogenic outer layer distributed over at least a portion of the device. | 05-28-2015 |
20150148883 | PLAIN WOVEN STENTS - Self-expandable, woven intravascular devices for use as stents (both straight and tapered), filters (both temporary and permanent) and occluders for insertion and implantation into a variety of anatomical structures. The devices may be formed from shape memory metals such as nitinol. The devices may also be formed from biodegradable materials. Delivery systems for the devices include two hollow tubes that operate coaxially. A device is secured to the tubes prior to the implantation and delivery of the device by securing one end of the device to the outside of the inner tube and by securing the other end of the device to the outside of the outer tube. The stents may be partially or completely covered by graft materials, but may also be bare. The devices may be formed from a single wire. The devices may be formed by either hand or machine weaving. The devices may be created by bending shape memory wires around tabs projecting from a template, and weaving the ends of the wires to create the body of the device such that the wires cross each other to form a plurality of angles, at least one of the angles being obtuse. The value of the obtuse angle may be increased by axially compressing the body. | 05-28-2015 |
20150320956 | SYSTEM AND METHOD FOR FABRICATING CUSTOM MEDICAL IMPLANT DEVICES - A method for creating tubular inserts is useful for creating custom fitted inserts that correspond to the anatomy of a patient and solve the problem of pressure points, wear of the implant, damage to surrounding tissue, and denting. Surface measurements of the affected portion of a patient's internal cavity are obtained. Those measurements are used to design a core. The core is 3D printed with a soluble material. The core is wrapped with a thin filament or film such that the contours from the core develop on the outer surface of the covering. The covering is hardened and the core is dissolved away, leaving a custom-made implant device that can be deposited in the patient's cavity. | 11-12-2015 |
20150328022 | MEDICAL DEVICE HAVING MAGNETICALLY EXPANDABLE FRAME - A stent, for example, is provided with a plurality of frame elements, which may have an undulating form. The stent is provided with a plurality of magnetic elements between adjacent stent elements. The magnetic elements on opposing circumferentially facing portions or sides of the strut elements have the same polarities so as to produce repulsive forces biasing the stent structure into a radially expanded configuration. The magnetic elements provide an alternative opening force on the stent, enabling the stent to be made of struts of thinner and weaker material or of a non-sprung material. The magnetic elements also provide a constant opening force in order to retain the stent reliably in position within a vessel. The stent could be made of a biodegradable material. | 11-19-2015 |
20150342760 | ANTI-MIGRATION STENT - Embodiments of the disclosure relate to devices, systems and methods of use and manufacture. One such device is a stent. The stent includes a stent body and a coating over at least a portion of the stent body. The coating includes a shape memory polymer having an outer surface. The outer surface defines a first configuration and a second configuration. In the first configuration the outer surface is smooth. In the second configuration, the outer surface includes a micro pattern. | 12-03-2015 |
20150366681 | STENT - A bioabsorable stent is disclosed. The stent is made of a polymer and/or non-polymer material and has an elongated body having a proximate end, a distal end, and at least one open channel formed on the exterior surface of the elongated body to provide fluid communication between the proximal end and the distal end. Also disclosed is a bioabsorable stent having an elongated center rod having a proximate end and a distal end and a plurality of leaflets extending outward from the center rod and forming channels between two neighboring leaflets to provide fluid communication between the proximal end and the distal end. | 12-24-2015 |
20150374518 | PERSONALIZED PROSTHESIS AND METHODS OF USE - A personalized prosthesis for implantation at a treatment site of a patient includes a self-expanding mesh or membrane having collapsed and expanded configurations. The collapsed configuration is adapted to be delivered to the treatment site, and the expanded configuration engages the personalized prosthesis with the treatment site. The mesh or membrane is personalized to match the treatment site in the expanded configuration, and has an outer surface that substantially matches the treatment site shape and size. The self-expanding mesh or membrane forms a central lumen configured to allow blood or other body fluids to flow therethrough. Methods of manufacturing and delivery of the personalized prosthesis are also disclosed. | 12-31-2015 |
20150374520 | SELF-EXPANDING STENT - The stent of this invention is a self-expanding stent created by a scaffolding lattice. The stent may be made from a nickel-titanium alloy. The lattice is formed from two different types of helices that proceed circumferentially in opposite directions along the longitudinal axis of the stent. The helices have no free ends. The first type of helix is formed by a series of undulations and the second type of helix is formed from a series of connection elements. The undulations may be in a zigzag or sinusoidal pattern. The connection elements connect the junction points lying on adjacent turns of the first type of helix. The junction points are formed by the ascending and descending arms of the undulations or zigzags. The ends of the stent may be formed by a closed circumferential element which is linked by connection elements to a transition zone. The transition zone is formed by a closed loop that connects directly to the first helix. The amplitude of the undulations or zigzags forming the transition zone increases from the closed loop to the point connecting the transition zone with the first type of helix. The closed circumferential element may be made from a radiopaque material. The scaffolding lattice design of the stent provides a stent having a high degree of flexibility as well as radial strength. | 12-31-2015 |
20150374521 | BIODEGRADABLE ENDOPROSTHESES AND METHODS FOR THEIR FABRICATION - The disclosure provides biodegradable implantable devices such as a stent comprising a biodegradable polymeric wherein the polymeric material is treated to control crystallinity and/or Tg. The stent is capable to expand at body temperature from a crimped configuration to a deployed diameter and have sufficient strength to support a body lumen. | 12-31-2015 |
20160015534 | STENT - A stent which improves safety by allowing a living body to be less affected even if a drug is detached. A stent has a strut that is formed in a linear shape, and that defines a cylindrical shape having an opening, a side surface coating member which coats at least a part of at least one of the side surfaces of the strut, the side surface coating member including a drug and a drug loading member which is a polymeric material for loading the drug, and an outer surface coating member which coats at least a part of the outer surface of the strut, the outer surface coating member including the drug without including the drug loading member. | 01-21-2016 |
20160030210 | COMPOSITE STENT - A biodegradable and/or bioabsorbable composite stent includes a bioabsorbable ceramic material coated with a biodegradable polymeric material. | 02-04-2016 |
20160038317 | IMPLANTABLE VASCULAR DEVICE HAVING LONGITUDINAL STRUTS - An implantable frame comprises a plurality of corner structures configured to decrease pressure to the vessel wall and define pulsatility enhancing windows of the implantable frame. The corner structures may comprise plurality of neighboring longitudinal struts that extend in a longitudinal direction of the blood vessel when placed to form the vessel wall to a substantially polygonal cross-section and distribute pressure loading of the corner structure among the plurality of neighboring longitudinal struts to improve biocompatibility. The corner structures also allow increased forming of the vessel wall and can provide stretching of the vessel wall to enhance pulsatility of the vessel wall. | 02-11-2016 |
20160038319 | ENDOVASCULAR GRAFT HAVING A CANNULATION POCKET - A stent graft for placement in a lumen of a patient is disclosed. The stent graft comprises: a main tubular body of a biocompatible graft material having a main lumen, the main tubular body having a proximal end and a distal end; a side arm extending from the main tubular body, the side arm having a side arm lumen, the side arm lumen being in fluid communication with the main lumen through a side arm opening in the main tubular body; and a cannulation pocket. The pocket comprises: an exit aperture positioned opposite the side arm opening; an entry aperture longitudinally spaced from the entry aperture in a direction toward the distal end of the main tubular body; and a wall, the wall laterally spaced from the main lumen so as to provide a guide surface for a cannula fed through the entry aperture. | 02-11-2016 |
20160113791 | Implants Having High Fatigue Resistance, Implant Delivery Systems, and Methods of Use - According to one aspect of the preset invention, a fatigue resistant stent includes a flexible tubular structure having an inside diameter, an outside diameter, and a sidewall therebetween and having apertures extending through the sidewall. According to other aspects of the invention, processes for making a fatigue resistant stent are disclosed. According to further aspects of the invention, delivery systems for a fatigue resistant stent and methods of use are provided. | 04-28-2016 |
20160143755 | SELF-EXPANDABLE STENT - A self-expandable stent includes a plurality of first wires and a plurality of second wires interwoven together. A first anchor member is attached to a distal end of one of the plurality of first wires. The distal end of the first anchor member is fixed to the distal end of the one of the plurality of first wires, but the proximal end is a free end and is not fixed to any of the plurality of first wires or to any of the plurality of second wires. Consequently, the self-expandable stent is capable of contacting a blood vessel wall or digestive organ wall at the optimal position when the self-expandable stent is expanded at the target site. A gap is not easily formed between the anchor member and the blood vessel wall or digestive organ wall, and thus the self-expandable stent is not easily dislocated from the target site. | 05-26-2016 |
20160193059 | INTRALUMINAL IMPLANTS AND METHODS | 07-07-2016 |
20170232156 | ANTI-THROMBOGENIC MEDICAL DEVICES AND METHODS | 08-17-2017 |