| 05th week of 2016 patent applcation highlights part 7 |
| Patent application number | Title | Published |
|---|
| 20160030140 | DENTAL IMPLANT SYSTEM HAVING ENHANCED SOFT-TISSUE GROWTH FEATURES - A dental implant system including an implant and an abutment is disclosed. The implant includes a generally cylindrical body, a central axis, a distal end for anchoring in a patient's bone and a proximal end opposing the distal end. The proximal end includes a roughened lateralized surface that surrounds an abutment-engaging region. The lateralized surface is disposed at a negative slope relative to the central axis. The abutment includes an upper portion for supporting a tooth-like prosthesis and a lower portion for engaging the abutment-engaging region of the dental implant. The diameter of the lower portion of the abutment is smaller than the diameter of the implant at its proximal end. The lower portion includes a first surface with a soft-tissue enhancing material. The first surface and the lateralized surface defining a circumferentially extending recess having a V-shaped cross-section for receiving and attachment to the soft tissue. | 2016-02-04 |
| 20160030141 | METHOD FOR MANIPULATING A DENTAL VIRTUAL MODEL, METHOD FOR CREATING PHYSICAL ENTITIES BASED ON A DENTAL VIRTUAL MODEL THUS MANIPULATED, AND DENTAL MODELS THUS CREATED - A 3D virtual model of an intra oral cavity in which at least a part of a finish line of a preparation is obscured is manipulated in virtual space by means of a computer or the like to create, recreate or reconstruct finish line data and other geometrical corresponding to the obscured part. Trimmed virtual models, and trimmed physical models, can then be created utilizing data thus created. The virtual models and/or the physical models may be used in the design and manufacture of copings or of prostheses. | 2016-02-04 |
| 20160030142 | Dental Crown Cementation Soft Tissue and Biologic Attachment Protective Membrane and Method of Use Thereof - A dental crown cementation soft tissue and biologic attachment protective membrane has a dental membrane and a membrane carrier. The dental membrane is attached within the membrane carrier for easy manual manipulation. The dental membrane is used during dental crown installation to prevent dental cement from leaking out from the interior cavity of the dental crown into the gingival sulcus and surrounding soft tissue. The dental membrane is placed atop a dental abutment onto which the dental crown is to be installed. The dental crown is pressed onto the abutment over the dental membrane, causing excess cement to be extruded from the interior cavity onto the dental membrane. The dental crown then has minimal excess cement. The dental crown is then removed as well as the dental membrane, the cement on the exterior crown surface is removed, and the adequately cemented dental crown is again attached to the dental abutment. | 2016-02-04 |
| 20160030143 | FOLDABLE AND FLEXIBLE ULTRASONIC VIBRATION MASK FOR TEETH CLEANING - A foldable and flexible ultrasonic vibration mask for cleaning teeth comprises two upper devices and two lower devices. Each upper device comprises a flexible substrate, coils configured to generate ultrasonic sound and formed on the flexible substrate, coils configured to generate audible sound and formed on the flexible substrate, a resonance chamber attached to the flexible substrate and including a magnetic alloy. Each lower device includes a flexible substrate, coils configured to generate ultrasonic sound and formed on the flexible substrate, and a resonance chamber attached to the flexible substrate and including a magnetic alloy. The flexible substrates of the two upper devices are fixed together. The flexible substrates of each upper device and a corresponding lower device are fixed together. The flexible substrates of the two lower devices are fixed together. | 2016-02-04 |
| 20160030144 | DIGITAL FACE BOW SYSTEM AND METHOD - A digital face bow system for capturing a patient's dento-facial characteristics by acquiring and registering data defining the tilt or slant of the occlusal or incisal plane of a patient's teeth in three planes of space in relation to the cranium, head and/or face. The system includes a substrate adapted to support bite registration material, and a digital multiple axis inclinometer coupled to the substrate for registering the orientation of the occlusal or incisal plane, where the midline of the patient's horizontal-facial plane is registered. An adjustable mounting platform is adapted to receive the substrate and replicate the inclination registered by the digital multiple axis inclinometer. | 2016-02-04 |
| 20160030145 | Safe Method For Bleaching Teeth - A safe method for bleaching teeth applies a thin film of a first bleaching composition having a high concentration of a bleaching agent to teeth to be bleached immediately followed by applying a second bleaching composition having a low concentration of a bleaching agent to teeth to be bleached. | 2016-02-04 |
| 20160030146 | VACCINE DELIVERY DEVICES - This document provides vaccine delivery devices and methods for vaccinating an animal (e.g., a mammal). For example, vaccine delivery devices that include a container having one or more openings, a vaccine depot located within the container, and a diffusion barrier located within the container in a manner such that material (e.g., an antigenic vaccine component) within the vaccine depot must pass through the diffusion barrier before reaching one of the openings are provided. | 2016-02-04 |
| 20160030148 | Implantable Reinforcement Prothesis, In Particular for Reinforcing the Abdominal Wall - The implantable reinforcement prosthesis, in particular for reinforcing the abdominal wall, comprises a reinforcement part ( | 2016-02-04 |
| 20160030149 | REINFORCEMENT DEVICE WITH DISSOLVABLE LAYER AND ITS USE - A reinforcement device for reinforcing tissues having one or more structural deficiencies includes a longitudinally-extending reinforcing layer for treating the structural deficiency, a plurality of spiked naps distributed across the reinforcing layer and projecting therefrom for adhering to the tissue, and a dissolvable matrix layer covering at least a portion of the reinforcing layer and a portion of the plurality of spiked naps. The matrix layer increases the time before the spiked naps substantially adhere to the tissue, thereby allowing the practitioner additional time to position the reinforcement device. | 2016-02-04 |
| 20160030150 | METHODS AND APPARATUS FOR DEPLOYING SHEET-LIKE MATERIALS - Implant delivery systems for delivering sheet-like implants include a delivery shaft, an implant expander, a sheath, and a sheet-like implant. In some embodiments, the delivery shaft has a proximal end and a distal end. The implant expander is mounted to the distal end of the delivery shaft. The implant expander includes a central portion and a plurality of leg portions radiating from the central portion. The implant expander is evertable between an unstressed configuration in which a distal surface of the implant expander defines a concave surface, and a first compact configuration in which the distal surface of the implant expander defines a convex surface. The implant expander has a first lateral extent when the implant expander is free to assume the unstressed configuration. The sheath defines a lumen having a lumen diameter. At least a portion of the delivery shaft is slidably disposed in the lumen. The lumen diameter is smaller than the first lateral extent of the implant expander so that the sheath holds the implant expander in the first compact configuration when slidably disposed therein. The sheet-like implant overlays at least a portion of the distal surface of the implant expander with portions of the sheet-like implant extending between the leg portions of the implant expander and the sheath. Methods of treating a rotator cuff of a shoulder are also disclosed. | 2016-02-04 |
| 20160030151 | FILTERS WITH ECHOGENIC CHARACTERISTICS - There are described a variety of intravascular filters have wherein at least a portion of the filter has been modified to provide an enhanced echogenic characteristic of the filter. | 2016-02-04 |
| 20160030152 | ENDOLUMINAL FILTER HAVING ENHANCED ECHOGENIC PROPERTIES - An endoluminal filter, comprising a first support member having a first end and a second end; and a second support member attached to the first end of the first support member or the second end of the first support member and forming a crossover with the first support member to form two loops one on either side of the crossover, wherein at least a portion of the first support member, the second support member, the first end, the second end or a region adjacent to the cross over or any portion of one of the above is modified to provide an enhanced echogenic characteristic of the endoluminal filter. A method of positioning a filter within a lumen, comprising advancing a sheath containing a filter through the lumen; deploying a portion of the filter from the sheath into the lumen to engage the lumen wall while maintaining substantially all of a material capture structure of the filter within the sheath; and deploying the material capture structure of the filter from the sheath to a position across the lumen, wherein any of the above steps are performed using an intravascular ultrasound system and the filter is modified to provided at least one echogenic characteristic. | 2016-02-04 |
| 20160030153 | EMBOLIC PROTECTION DURING PERCUTANEOUS HEART VALVE REPLACEMENT AND SIMILAR PROCEDURES - Various devices are described to provide filtering of flow from the aorta to the left carotid artery and the right carotid artery. The filters can be brought into a desired position through one or more peripheral arteries. A single filter device can provide the desired filtering or a plurality of devices can be used. In particular a single filter device can span between the brachiocephalic artery and the left carotid artery. These filter devices can be used effectively to capture emboli generated during procedures on the heart so that emboli do not travel to the patient's brain where the emboli can cause a stroke or other adverse event. In particular, these filters can be used during percutaneous procedures on the heart, such as endovascular heart valve replacement. | 2016-02-04 |
| 20160030154 | PROSTHETIC DEVICE INCLUDING ELECTROSTATICALLY SPUN FIBROUS LAYER AND METHOD FOR MAKING THE SAME - In accordance with certain embodiments of the present disclosure, a process of forming a prosthetic device is provided. The process includes forming a dispersion of polymeric nanofibers, a fiberizing polymer, and a solvent, the dispersion having a viscosity of at least about 50,000 cPs. A tubular frame is positioned over a tubular polymeric structure. Nanofibers from the dispersion are electrospun onto the tubular frame to form a prosthetic device. The prosthetic device is heated. | 2016-02-04 |
| 20160030155 | Aneurysm Graft With Stabilization - The present invention provides methods and apparatus for the endoluminal positioning of an intraluminal prosthesis at a target location within a body lumen. The device may comprise a porous, multi-layer prosthesis that can include stabilization members for stabilizing the placement of the device at the site. Various components can have different densities or pore sizes. | 2016-02-04 |
| 20160030156 | System and Method for Load Balancing in Knee Replacement Procedures - The present disclosure relates to a system and method of knee ligament balancing for knee replacement procedures. The disclosure provides a system of components to implant to achieve ligament balancing. In addition, instruments and methods are provided to achieve the desired balance of the ligaments before final fixation. | 2016-02-04 |
| 20160030157 | MEDICAL DEVICE DELIVERY SYSTEM AND METHOD - A tendon repair implant delivery system and methods incorporating a guide member having a temporary fixation member on or adjacent to the distal end. The point of fixation defines a target site for placement of the tendon repair implant which is subsequently affixed to the tendon. | 2016-02-04 |
| 20160030158 | TISSUE GRAFT FIXATION - A tissue graft fixation device including a body having an upper and lower surface, a first end portion, a second end portion, and an intermediate portion extending between the first and second end portions, the intermediate portion comprising at least two tabs extending transverse to the intermediate portion, the intermediate portion defining at least one hole located between the at least two tabs, and each of the at least two tabs comprising a keel extending transverse to the intermediate portion and including a cutting edge. | 2016-02-04 |
| 20160030159 | TISSUE CAPTURING BONE ANCHOR - A bone anchor configured for use in anchoring an implanting portion to an anchor point. A bone anchor can be of particular use in anchoring soft tissue to a bone. A bone anchor can have a wire loop and a suture. The wire loop of the bone anchor can be configured to capture a suture and to pull a portion of the suture through a hole in the anchor body aiding in anchoring an item, such as tissue to a bone. Methods of using the bone anchor with a suture and a wire loop to attach an item are disclosed. | 2016-02-04 |
| 20160030160 | PIEZOELECTRIC SENSOR FOR VISION CORRECTION - The present invention will provide a vision correction device which utilizes the movements of the eye to correct the focus of the user without the need of surgical procedures. More specifically, the present invention will detect the movement of the ciliary muscle and adaptively modify the shape of an artificial lens positioned inside or outside of the eye to adjust the focus of the lens. This adjustment will occur very rapidly and coincide with the ciliary muscle's attempt to focus the crystalline lens of the eye. | 2016-02-04 |
| 20160030161 | ACCOMMODATING INTRAOCULAR LENS DEVICE - An accommodating intraocular lens (IOL) can be implanted either alone or as part of a two-part lens assembly. The IOL comprises an optic, a flexible membrane and a peripheral edge coupling the optic and the flexible membrane. The peripheral edge comprises an external circumferential surface having a height and a force transmitting area defined along a portion of the height of the external circumferential surface. A closed volume spaces apart the optic and the flexible membrane. The optic is axially displaced and the flexible membrane changes in curvature about a central axis when a radial compressive force is applied to the force transmitting area. A volume defined by the closed volume remains fixed when the optic is axially displaced and the flexible membrane changes in curvature and/or when the radial compressive force is applied to the force transmitting area. | 2016-02-04 |
| 20160030162 | Intraocular Lens with Electricity Generator and Additional Functional Systems - An accommodating intraocular lens combination with two optical elements which move versus each other. The optical elements have such a shape that the combination provides variable focusing power at different positions of at least one of the optical elements relative to the other optical element. The lens combination also includes an electricity generator and a functional system, which can be a, micro, mano meter system, or, a micro glucose measurement system, or, a micro intraocular driver system for amplification of accommodation movements. The lens combination includes a wireless connection component to send or receive information from or to, for example, a smart-phone. | 2016-02-04 |
| 20160030163 | Surgical Apparatus and Method Of Implanting The Same - A surgical apparatus is provided for implantation into organic tissue for use with an implant having one or more stabilizing haptics. The surgical apparatus has a ring-like body for stabilizing organic tissue. The body has an outer surface and one or more abutments extending from the outer surface. The abutment is for engaging the stabilizing haptics of the implant to inhibit movement of the implant within the organic tissue. | 2016-02-04 |
| 20160030164 | EXPANDABLE MEMBER FOR DEPLOYING A PROSTHETIC DEVICE - An apparatus and method for delivering a prosthetic device through the vasculature of a patient includes a radially expandable member coupled to the distal end of an elongate shaft. The expandable member has an open frame configuration and an outer mounting surface for mounting the prosthetic device in a collapsed state thereon. The expandable member expands radially outwards from a first configuration to a second configuration to expand a prosthetic device mounted thereon. | 2016-02-04 |
| 20160030165 | Means for Controlled Sealing of Endovascular Devices - Expandable sealing means for endoluminal devices have been developed for controlled activation. The devices have the benefits of a low profile mechanism (for both self-expanding and balloon-expanding prostheses), contained, not open, release of the material, active conformation to the “leak sites” such that leakage areas are filled without disrupting the physical and functional integrity of the prosthesis, and on-demand, controlled activation, that may not be pressure activated. | 2016-02-04 |
| 20160030166 | APPARATUS, SYSTEM, AND METHOD FOR TREATING A REGURGITANT HEART VALVE - An apparatus for treating regurgitation of blood through a diseased heart valve having at least two leaflets includes a lollipop-shaped body member having a proximal end portion, a distal end portion, and an intermediate portion extending between the end portions. The intermediate portion includes an expandable occluding member having an adjustable diameter so that, during at least a portion of the cardiac cycle, at least one of the heart leaflet coapts with a portion of the occluding member to mitigate or prevent regurgitation of blood through the diseased heart valve. The proximal end portion is physically connected to the occluding member and includes a connecting mechanism for operably mating with an adjustment member for adjusting the position and diameter of the occluding member within the diseased heart valve. The distal end portion includes an anchoring member for securing the apparatus in a heart chamber containing the diseased heart valve. | 2016-02-04 |
| 20160030167 | Transcatheter Stent-Valves and Methods, Systems and Devices for Addressing Para-Valve Leakage - Some embodiments of the present disclosure provide a stent-valve for transcatheter implantation to replace a cardiac valve. In some embodiments, the stent valve being compressible to a compressed state for delivery, and expandable to an operative state for implantation. In some embodiments, the stent-valve comprises a stent, a plurality of leaflets for defining a prosthetic valve, an inner skirt, an outer skirt, and a paravalve seal for sealing against surrounding tissue. In some embodiments, the paravalve seal comprising material that swells in response to contact with blood or components thereof. | 2016-02-04 |
| 20160030168 | PROSTHETIC HEART VALVE AND METHOD - A prosthetic heart valve comprises a radially crimpable and radially expandable, net-like, annular support frame and a valve assembly disposed therein, the valve assembly comprising a conduit tapering from an inlet towards an outlet thereof. Some embodiments or the support frame comprise a proximal portion and a distal portion, a diameter of the proximal portion smaller than a diameter of the distal portion. The proximal portion is dimensioned for deployment in an annulus of a native aortic valve and a distal portion for deployment in an ascending aorta. Some embodiments of the conduit comprise a support construction with a three-cusp, crown-shaped cut line, the support construction sutured to the support frame around a bottom portion thereof and around the cut line. A method for using the prosthetic heart valve to replace a defective native aortic valve uses a minimally invasive procedure. | 2016-02-04 |
| 20160030169 | DUAL FRAME STENT AND VALVE DEVICES AND IMPLANTATION - A device for placement in a biological tissue fluid conduit includes an outer frame, multiple stabilizer arms, an inner frame, and a valve. The outer frame circumferentially surrounds a longitudinal axis and defines an interior passageway. The outer frame has an interior side facing the longitudinal axis and passageway, and an exterior side opposite the interior side. The stabilizer arms extend outward from the outer frame. The inner frame is positioned in the passageway and circumferentially surrounds the longitudinal axis with at least a longitudinal portion of the inner frame circumferentially surrounded by the outer frame. The inner frame has an exterior side facing the interior side of the outer frame. The valve is housed by the inner frame and is configured to restrict fluid flow through the passageway in at least one of two longitudinal directions. | 2016-02-04 |
| 20160030170 | SELF-ACTUATING SEALING PORTIONS FOR A PARAVALVULAR LEAK PROTECTION - A prosthetic heart valve ( | 2016-02-04 |
| 20160030171 | CATHETER-GUIDED REPLACEMENT VALVES APPARATUS AND METHODS - The present invention is a replacement mitral valve suitable for catheter-based deployment. The replacement mitral valve has structure and dimensions that are uniquely suited to engage the annulus surrounding the native mitral valve and to restore normal function to a diseased valve. The invention describes the structures and functions of a replacement mitral valve and methods that are adapted for minimally invasive, catheter-based deployment of the valve. | 2016-02-04 |
| 20160030172 | VALVE ASSEMBLY FOR CRIMP PROFILE - A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient. | 2016-02-04 |
| 20160030173 | PROSTHETIC HEART VALVE INCLUDING STENT STRUCTURE AND TISSUE LEAFLETS, AND RELATED METHODS - A method of making a prosthetic heart valve may include providing an annular stent having a plurality of annularly spaced commissure portions having tips, covering each of the tips with a first fabric cover, covering the first fabric covers and the remainder of the stent with a second fabric cover, covering the second fabric cover with a first tissue membrane, and covering the outside of the first tissue membrane with a second tissue membrane, the second tissue membrane forming leaflet portions that extend inwardly between the commissure portions. | 2016-02-04 |
| 20160030174 | ARTIFICIAL VALVE FOR IMPLANTATION - An artificial heart valve consists of two or more valve members ( | 2016-02-04 |
| 20160030175 | METHOD AND APPARATUS FOR THERAPY OF MITRAL VALVE - Devices and methods are described for treating a mitral valve defect. The device described includes features that allow the device to conform to the actual pathology of the valve, rather than attempting to replicate a healthy valve (which the patient does not have). In this way, the device allows the patient's actual value to work as well as possible, given the valve's diseased condition. The actual pathology of the valve is accommodated by providing for multiple dimensions of adjustability of the device, including adjustability of the size (e.g., diameter) of the device as well as adjustability of the elevation or inclination of one portion of the device (e.g., the portion supporting the posterior leaflet) with respect to another portion of the device. | 2016-02-04 |
| 20160030176 | Implant and method for improving coaptation of an atrioventricular valve - The invention relates to an implant and a method for improving coaptation of an atrioventricular valve, the atrioventricular valve having a native first leaflet, a native second leaflet and an annulus. The implant comprises a support structure and a flexible artificial leaflet structure mounted to the support structure and shaped to coapt with the native second leaflet. | 2016-02-04 |
| 20160030177 | METHOD AND APPARATUS FOR MEASURING CONTRACTION CHARACTERISTICS OF ENGINEERED HEART TISSUE CONSTRUCTS - The invention is directed to a novel method for measuring contraction characteristics of engineered heart tissue constructs ( | 2016-02-04 |
| 20160030180 | FASTENING CERAMIC COMPONENTS - A ceramic component to be securely connected to an additional component in force-locked manner. A joint prosthesis comprising a ceramic sphere ( | 2016-02-04 |
| 20160030181 | Implantable medical device and method of implanting the medical device - An implantable medical device for implantation in a mammal joint having at least two contacting surfaces is provided. The medical device comprises; an artificial contacting surface adapted to replace at least the surface of at least one of the mammal's joint contacting surfaces, wherein the artificial contacting surface is adapted to be lubricated, when implanted in said joint. Furthermore the medical device comprises at least one inlet adapted to receive a lubricating fluid from a reservoir, at least one channel at least partly integrated in the artificial contacting surface in connection with the at least one inlet for distributing the lubricating fluid to the surface of the artificial contacting surface. The medical device could be adapted to be operable by an operation device to receive the distributed lubricated fluid from a reservoir. | 2016-02-04 |
| 20160030182 | PROSTHETIC COMPONENT WITH CROSSLINKED POLYMER WEAR ZONE AND EDGE PROTECTION - A method of manufacturing a prosthetic component comprises providing crosslinked polymer in a mould and moulding non-crosslinked polymer to a free edge of the crosslinked polymer to form a hybrid component. A portion of the crosslinked polymer and a portion of the non-crosslinked polymer is then removed so as to form a prosthetic component having a full thickness crosslinked wear zone and at least one non-crosslinked edge. | 2016-02-04 |
| 20160030183 | SYSTEM OF DESIGNING A GUIDE TOOL AND/ OR SURGICAL KIT TOOLS AND/OR AN IMPLANT COMPRISING A POSITIONING MARK - A design method for designing a guide tool including a guide channel for use during cartilage repair in a joint is disclosed. The design method includes: selecting a direction along a joint axis indicating placement of the guide tool in the joint; and placing a positioning mark on the guide tool. The positioning mark is designed to be aligned with the center of said guide channel on a determined joint axis direction and thereby indicating a placement direction of the guide tool in relation to the selected joint axis during use of the guide tool. A design method of insert tools and/or an implant comprising positioning marks and also the guide tool, implant and insert tools designed using this method are also disclosed. | 2016-02-04 |
| 20160030184 | Implant with multi-directional pivoting - Implant with multi-directional pivoting has a first component including a first articular surface and a fore-to-aft and side-to-side rotation device; and a second component including a second articular surface for mating with the first articular surface and a rotation device receptacle. The first component can be mated to the second component through cooperation of the rotation device and the rotation device receptacle, and the first component can cooperate with the second component in contact of the first and second articular surfaces and in articulation of the joint when the first component is mated to the second component. The implant can be an artificial joint which generally has natural load transfer capability. In a particular embodiment, the joint is a knee prosthesis; therein, the first and second components are femoral and tibial components, with the first articular surface a femoral condylar surface and the second articular surface a tibial condylar mating surface. In such a knee, the fore-to-aft component can be considered flexion, with the side-to-side component considered version. As well, a knee prosthesis can be provided with a device to support the patella on a smooth counter surface from full extension to flexion well past | 2016-02-04 |
| 20160030185 | MODULAR FEMORAL PROVISIONAL - A provisional prosthetic system that replicates the characteristics of a corresponding, nonprovisional femoral prosthesis. The provisional prosthetic system may include a frame component and a shell component. The frame component of the provisional prosthetic system may be configured to be attached directly to a resected femur. In one exemplary embodiment, the frame component is impacted onto the resected femur to firmly seat therewith. Once the frame component is secured to the resected femur, a shell component of the provisional prosthetic system may be positioned on and secured to the frame component. In one exemplary embodiment, the frame component is made from a metallic material. This allows for the frame component to maintain the rigidity necessary to facilitate proper trialing. In another exemplary embodiment, the shell component is a plastic. | 2016-02-04 |
| 20160030186 | METHOD OF IMPLANTING A UNICONDYLAR KNEE PROSTHESIS - A method of implanting a lateral unicondylar knee prosthesis in a lateral articulating portion of a femur having a lateral condyle for engagement with a tibia, the method including the steps of: bending a patients knee such that the knee is not in full extension; making an incision through the skin, muscle, and other soft tissue until the damaged bone surfaces are exposed; resecting an end portion of the lateral tibia; resecting an end portion of the lateral femoral condyle; attaching a tibial prosthetic component to the resected end portion of the tibia; attaching a lateral femoral condyle prosthetic component to the resected end portion of the lateral femoral condyle; determining the thickness of a mobile bearing member with the knee in full extension; and inserting the mobile bearing member between the tibial prosthetic component and the femoral prosthetic component. | 2016-02-04 |
| 20160030187 | SHOULDER PROSTHESIS WITH VARIABLE INCLINATION HUMERAL HEAD COMPONENT - Methods and devices are disclosed for joint (e.g., shoulder) arthroplasty. In one aspect, there is provided a device for determining inclination and/or version of a prosthetic head with respect to a prosthetic stem. In another aspect, there is provided a joint (e.g., shoulder) prosthesis. In another aspect, there is provided a method for setting an inclination angle and/or a version angle of a prosthetic head with respect to a stem implanted or to be implanted in a bone of a joint (e.g., shoulder). | 2016-02-04 |
| 20160030188 | INTERBODY IMPLANTS AND GRAFT DELIVERY SYSTEMS - According to some embodiments, a method for promoting spinal fusion using a spinal implant comprises providing a spinal implant, wherein the spinal implant comprises at least one internal chamber being is adapted to receive at least one graft and/or other fill material. In some arrangements, one or more walls of the spinal implant comprise at least one opening or hole that places the internal chamber in fluid communication with an exterior area or portion of the spinal implant. The method additionally includes positioning the spinal implant between two adjacent vertebrae of a patient and directing at least one graft and/or other fill material into the internal chamber of the spinal implant through the access port. | 2016-02-04 |
| 20160030189 | EXPANDABLE INTER-BODY FUSION DEVICES AND METHODS - An expandable curved inter-body fusion device is presented. The expandable curved inter-body fusion device can have a first plate, a second plate, and an insert positioned substantially therebetween the first plate and the second plate. The first plate, the second plate, and the insert define an interior cavity. Moving the insert longitudinally with respect to the first and second plates increases or decreases the distance of the first plate with respect to the second plate, effectively expanding the inter-body fusion device and increasing the volume of the interior cavity. | 2016-02-04 |
| 20160030190 | EXPANDABLE INTERVERTEBRAL CAGE ASSEMBLIES - An expandable assembly for insertion into an intervertebral space is presented. The assembly, in particular aspects, includes an elongate body comprising an upper portion and a lower portion, wherein the elongate body defines an internal longitudinal channel extending from a proximal opening to a distal cavity. The assembly may include an expander that is sized and shaped for insertion into the distal cavity, thereby selectively expanding the upper portion away from the lower portion. The elongate body may also include one or more bone graft windows a cap that is sized and shaped for insertion into the proximal opening. | 2016-02-04 |
| 20160030191 | BONE FUSION DEVICE - A bone fusion device provides stability to bones during a bone fusion period. The bones include, for example, the vertebrae of a spinal column. The bone fusion device comprises one or more extendable tabs attached to the bone fusion device by associated rotating means. The bone fusion device is preferably inserted by using an arthroscopic surgical procedure. During arthroscopic insertion of the device, the tabs are pre-configured for compactness. In this compact configuration, the tabs are preferably deposed along and/or within an exterior surface of the bone fusion device. After the bone fusion device has been positioned between the bones, one or more tab(s) are extended. In the preferred embodiment, the position of each tab is related to a positioning element and extending blocks. Typically, the tabs advantageously position and brace the bone fusion device in the confined space between the bones until the bones have fused. | 2016-02-04 |
| 20160030192 | Articulating Disc Implant - An intervertebral disc implant for use in the spine including a first part and a second part, wherein the first part and second part are configured as a joint prosthesis for the spine. The first part includes one of a concave or convex articulating surface and the second part includes one of the other concave or convex articulating surface. One of the concave or convex articulating surfaces is preferably elliptically shaped in at least one direction and does not match and is different than one of the other concave or convex articulating surfaces. | 2016-02-04 |
| 20160030193 | ARTIFICIAL DISC REPLACEMENTS WITH NATURAL KINEMATICS - This invention improves upon prior art total disc replacements (TDRs) by more closely replicating the kinematics of a natural disc. The preferred embodiments feature two or more fixed centers of rotation (CORs) and an optional variable COR (VCOR) as the artificial disk replacement (ADR) translates from a fixed posterior COR that lies posterior to the COR of the TDR to facilitate normal disc motion. The use of two or more CORs allows more flexion and more extension than permitted by the facet joints and the artificial facet (AF). AF joint-like components may also be incorporated into the design to restrict excessive translation, rotation, and/or lateral bending. | 2016-02-04 |
| 20160030194 | INTERVERTEBRAL CAGE AND METHOD OF TREATING VERTEBRAE WITH AN INTERVERTEBRAL CAGE - The present disclosure provides an intervertebral cage including superior and inferior members each including an engagement surface for engaging a corresponding vertebrae. The intervertebral cage also includes a posterior member that extends between a posterior end of the superior and inferior members and spaces them from each other in a superior-inferior direction. The superior and inferior members extend in a posterior-to-anterior direction from the posterior member and define anterior free ends to form a substantially open anterior end between the superior member and the inferior member in a posterior-anterior direction. The engagement surfaces of the superior and inferior members substantially diverge from each other in the superior-inferior direction along the posterior-to-anterior direction. The superior and inferior members each include first apertures extending therethrough in the superior-inferior direction that define a pathway through the intervertebral cage in the superior-inferior direction. | 2016-02-04 |
| 20160030195 | SURGICAL INSTRUMENT SYSTEM AND METHOD - A surgical instrument includes a body extending between a first end and a second end and includes at least one mating element engageable with an interbody implant. A first member is disposed with the body and engageable with the interbody implant to move the interbody implant between a first configuration and a second, expanded configuration. A second member is disposed with the body and engageable with the interbody implant to fix the interbody implant in a selected second configuration. Systems and methods are disclosed. | 2016-02-04 |
| 20160030196 | Customized Surgical Guide - Customized surgical guide for guiding a bone implant to a predetermined location on the bone during a surgical procedure, wherein the guide comprises a body comprising at least one implant contacting surface and at least one patient specific bone contacting surface, wherein the implant contacting surface is arranged to contact the implant for ensuring a unique and stable fit between the guide and the implant, and wherein the bone contacting surface is arranged to contact the bone for ensuring a unique and stable fit of a combination of the guide and the implant on the predetermined location on the bone. | 2016-02-04 |
| 20160030197 | SURGICAL METHOD FOR IMPLANTING A STEMLESS HUMERAL COMPONENT TO THE HUMERUS OF A PATIENT - A stemless humeral component for replacing the humeral head of a patient's humerus includes a support flange having a number of cantilevered legs extending distally away from a bottom surface thereof. Instruments and methods for surgically installing the stemless humeral component are also disclosed. | 2016-02-04 |
| 20160030198 | FEMORAL COMPONENT TRIAL FOR KNEE JOINT - A femoral component trial for a knee joint of the present invention includes a trial body. The trial body includes a medial condyle and a lateral condyle that are located away from each other on an external surface, a through hole that is located between the medial condyle and the lateral condyle and has an approximately rectangular shape whose long side is an outer edge of an inner wall located along a back-and-forth direction and whose short side is an outer edge of an inner wall located along a right-and-left direction in an external surface view, a first guide slit that is located ahead of and above the through hole and extends in the right-and-left direction, and four second guide slits respectively extending from four corner parts of the through hole and along the long side. | 2016-02-04 |
| 20160030199 | IMPLANT TRIALLING - A trial implant system and method of trialling are described. A stem prosthetic implant ( | 2016-02-04 |
| 20160030200 | IMPLANT TRIALLING - A trial implant system and method of trialling are described. The trial implant system comprises a stem component ( | 2016-02-04 |
| 20160030201 | Powered Orthotic System for Cooperative Overground Rehabilitation - A powered orthotic system, such as an exoskeleton, is employed for rehabilitation purposes by adapting and adjusting to real-time needs in a rehabilitation situation whereby the system can be initially controlled to perform gait functions for a wearer based on a predetermined level of assistance but the predetermined level of assistance can be varied, based on one or more rehabilitation parameters or specific needs of the wearer undergoing therapy, through the application and adjustment of appropriate variables associated with operation of the system. | 2016-02-04 |
| 20160030202 | Actuator Control System and Related Methods - An actuator control system includes a motorized joint having first and second members rotatable relative to one another. An actuator is coupled with the motorized joint and is configured to rotate the first member relative to the second member in response to an input including a voltage, a current, or any combination thereof. A controller is coupled with the actuator and is configured to control the input using a control algorithm. The control algorithm controls the input based upon a mathematical model of biological muscle actuation that models titin as a filament which winds around actin during muscle actuation. In implementations the mathematical model includes mathematical representations of a contractile element, a viscous damping element in parallel with the contractile element, and a spring in series with the contractile element through a pulley and simultaneously in parallel with the contractile element. | 2016-02-04 |
| 20160030203 | CONTROL OF A PASSIVE PROSTHETIC KNEE JOINT WITH ADJUSTABLE DAMPING - The invention relates to the control of a passive prosthetic knee joint with adjustable damping in the direction of flexion such that a prosthetic unit attached to the knee joint can be adapted for climbing stairs. | 2016-02-04 |
| 20160030204 | PROSTHETIC SUSPENSION MOUNTING ASSEMBLY - A prosthetic suspension-mounting system which employs an improved flathead bolt and socket centering block combination for securement of an amputee-limb enveloping liner within a prosthesis. The liner has a strap fixedly attached on the bottom end of the liner by a flathead bolt. The mounting system also includes a containment socket for seating the liner in the prosthesis using the head of the flathead bolt as a bearing surface against a floor of the socket. The containment socket has a slot there through at a position corresponding to the strap of the liner. The socket is provided with a disk-shaped recess having a flat floor, and the liner is provided with a distal flathead bolt having a flat head to provide a direct bearing surface against the floor of the socket. This provides a delimited bearing surface to keep the liner substantially centered within the prosthesis while still affording a lateral degree of freedom to avoid concentration of lateral forces. | 2016-02-04 |
| 20160030205 | Prosthetic Limb Heating Apparatus - A prosthetic limb heating apparatus for use with a prosthetic assembly includes a sleeve having a side wall that defines open upper and lower ends. The upper end is configured to receive an upper limb portion and prosthetic liner into the sleeve. The open lower end is configured to allow the upper limb portion to pass therethrough but not the prosthetic liner such that the prosthetic liner is nested in the interior area. An electrically conductive wire is situated on the sleeve and extends circuitously thereabout, the conductive wire having opposed first and second ends. A battery is coupled to the side wall of the sleeve and electrically connected to the first and second ends of the conductive wire so as to selectively energize the conductive wire. The conductive wire imparts heat to the prosthetic liner when the liner is nested within the sleeve and the conductive wire is energized. | 2016-02-04 |
| 20160030206 | Liner for Prosthetic Limb - The present invention relates to a liner for limb prosthesis ( | 2016-02-04 |
| 20160030207 | PROSTHESIS COOLING SYSTEM - A prosthesis cooling system may comprise one or more thermoelectric cooling devices embedded in a prosthesis socket, a power source, and a power control circuit. The cooling system may use active or passive cooling, and may use a closed-loop temperature control system. | 2016-02-04 |
| 20160030208 | MEDICAL DEVICE - Novel devices and methods for implanting medical stents are provided. A novel apparatus, which may be in a first compressed position, may be inserted into the artery, such as by being positioned over a catheter. The apparatus may be expanded to a second position. In one embodiment, the apparatus is configured to expand away in two substantially opposing directions along a second axis away from the longitudinal axis. The second axis may be perpendicular to the longitudinal axis. The apparatus may include markers that are detectable to determine the orientation of the catheter or the apparatus and/or assist in the determination of the type or size of stent to utilize. | 2016-02-04 |
| 20160030209 | MULTI-COMPONENT STENT-GRAFT SYSTEM FOR AORTIC DISSECTIONS - A generally tubular stent-graft ( | 2016-02-04 |
| 20160030210 | COMPOSITE STENT - A biodegradable and/or bioabsorbable composite stent includes a bioabsorbable ceramic material coated with a biodegradable polymeric material. | 2016-02-04 |
| 20160030211 | IMPLANTABLE PROSTHESIS WITH RADIOPAQUE PARTICLES AND METHOD OF MAKING SAME - An implantable prosthesis can comprise a strut having a lumen, radiopaque particles within the lumen, and a polymer binder. The polymer binder retains the radiopaque particles within the lumen. The strut may have side holes through which a therapeutic agent may pass and through which the radiopaque particles are incapable of passing. The polymer binder may be absent or optional. The radiopaque particles can have sizes that prevent them from escaping out of the lumen through the side holes. The radiopaque particles placed within the lumen can improve visualization of the prosthesis during an implantation procedure. | 2016-02-04 |
| 20160030212 | RUBBER TOUGHENED BIORESORBABLE POLYMER PERIPHERAL SCAFFOLDS - Bioabsorbable scaffolds are disclosed with a rigid polymer component and a rubbery polymer component. The rubbery polymer component is miscible, partially miscible, or immiscible with the rigid polymer component. | 2016-02-04 |
| 20160030213 | Bend-Capable Tubular Prosthesis - A tubular prosthesis having a succession of turns around a longitudinal axis includes connectors between adjacent turns distributed around the circumference of the prosthesis. Each turn includes struts interspersed by inflection zones located at the axial ends of each turn such that, when the prosthesis expands radially, gaps open up between adjacent struts of each of the turn. The inflection zones are distributed regularly around the circumference so that the gaps are substantially the same size as each other around the circumference of the turn. The prosthesis may include a turn that exhibits a stagger zone within which the gap between adjacent struts is of an individual size different from that common to the other gaps of that turn. The inflection zones in that turn that lie circumferentially next to the stagger zone are displaced out of facing relationship with corresponding zones of inflection in the adjacent turn. | 2016-02-04 |
| 20160030214 | METHODS FOR UNIFORM CRIMPING AND DEPLOYMENT OF A POLYMER SCAFFOLD - A medical device-includes a scaffold crimped to a catheter having an expansion balloon. The scaffold is crimped to the balloon by a process that includes one or more balloon pressurization steps. The balloon pressurization steps are selected to enhance scaffold retention to the balloon while retaining, at least partially, the original balloon folds as the balloon is pressurized and de-pressurized within a crimper head. By at least partially retaining the original balloon folds, a uniformity of scaffold expansion by the balloon is improved. | 2016-02-04 |
| 20160030215 | STENT-GRAFT WITH POSITIONING ANCHOR - A positioning anchor is provided for a stent-graft for implantation to treat a damaged body lumen. The positioning anchor is generally tubular surrounding a primary fluid conduit. Arms extend laterally from the generally tubular structure of the anchor surrounding lateral fluid conduits. The form of these arms is preferably custom configured to match a particular patient's luminal geometry. The anchor thus fits within the luminal geometry to remain in a desired fixed position for implantation of the anchor and any stent-graft coupled to the anchor. The anchor is most preferably formed with two walls having a void therebetween which can be filled with fixation media to further secure the anchor at the desired implantation site. A lumen shaper balloon and delivery catheter are also disclosed for proper delivery, expansion and inflation of the positioning anchor and stent-graft elements according to this invention. | 2016-02-04 |
| 20160030216 | METHODS FOR CRIMPING A POLYMERIC SCAFFOLD TO A DELIVERY BALLOON AND ACHIEVING STABLE MECHANICAL PROPERTIES IN THE SCAFFOLD AFTER CRIMPING - A medical device-includes a polymer scaffold crimped to a catheter having an expansion balloon. The scaffold is crimped to the balloon by a process that includes inflating the delivery balloon during a diameter reduction to improve scaffold retention. A crimping temperature is maintained at about the onset of glass transition of the polymer material to facilitate more rapid stabilization of mechanical properties in the scaffold following crimping. | 2016-02-04 |
| 20160030217 | Crush Recoverable Polymer Scaffolds - A method of manufacturing a stent is disclosed. The stent includes a minimum crimped diameter such that in the minimum crimped diameter, a pair of stent rings, between which marker support structures reside, do not make contact with the marker support structures. The crimped profile of the stent of the present invention can be as small as the crimped profile of a same stent but without the marker support structures. | 2016-02-04 |
| 20160030218 | STENT GRAFT ADAPTOR - A stent graft adaptor has an outer graft tube and an inner graft tube with the inner graft tube substantially concentric with and within the outer graft tube. A joining member extends between the inner tube and the outer tube. The joining member can be a continuous fold of graft material extending from a proximal end of the outer tube to a proximal end of the inner tube. The inner tube has at least one self expanding stent on an outer surface thereof and the outer graft tube has at least one self expanding stent on an inner surface. The outer surface of the outer tube provides a sealing surface to engage against the wall of a vessel and the inner tube provides a sealing surface to engage with a corresponding sealing surface of a stent graft deployed through it. The outer sealing surface can include barbs. | 2016-02-04 |
| 20160030219 | Upper Stomach Gastric Implants - A variety of passive intragastric implant devices for obesity treatment are disclosed. Such passive devices do not autonomously change shape, but instead react within the stomach to induce satiety. The devices may provide slowed entry into the stomach, thus reducing the intake capacity. Additionally, the devices may contact areas within the stomach, such as the cardia surrounding the esophageal sphincter, to stimulate satiety-inducing nerves. Some devices combine two or more of these satiety-inducing features. Methods of implant are disclosed including compressing the devices within a delivery tube and transorally advancing the devices through the esophagus to be deployed within the stomach. Removal of the devices occurs in the reverse. The implants are formed of materials that permit the implant to be compressed into a substantially linear transoral delivery configuration and that will resist degradation over a period of at least six months within the stomach | 2016-02-04 |
| 20160030220 | Magnetic Device To Control Obesity And Related Method Of Use - A medical device includes an outer shell defining a cavity, wherein the shell is movable between a deformed and unstressed state, a magnet disposed within the cavity, and a filler material carried within the cavity conforming to the interior shape of the shell in the unstressed state and being capable of holding its shape in the deformed state. The filler material converts from the deformed state to the unstressed state at a temperature not greater than human body temperature. | 2016-02-04 |
| 20160030221 | INTERNAL COVERING MEMBRANE OF DUODENUM - A duodenum internal covering membrane is disclosed. The covering membrane is made of a biocompatible material and mainly comprises an elastic ampulla and a tubular part, wherein the ampulla is positioned in the duodenal bulb, the tubular part can extend to the jejunum, the ampulla contains a wavy or V-shaped or trapezoidal or city wall-shaped elastic ring which is continuously encircled, the elastic ring is made of a memory or non-memory biocompatible material, peaks, valleys and bent angles of the elastic ring are single-circle coil springs with outward anchor hooks, the single-circle coil springs on the lower edge are penetrated and wound with recovery threads, the upper edge of the ampulla is a wavy or V-shaped or trapezoidal or city wall-shaped elastic membrane, the elastic ring and the ampulla comply with the motion of the duodenum and the bulb as a whole, and the ampulla and the tubular part can be closed up or folded into the shape of a ball or cylinder or capsule or spindle. The single-circle coil springs have strong elasticity, weak sharp injuries and good fixation for the recovery threads attached thereon, thereby being conductive to anatomical structure and basic physiological functions of the duodenum. The covering membrane within the duodenum of the present invention can be prepared into a medical device for preventing and treating obesity and diabetes. | 2016-02-04 |
| 20160030222 | Ankle-Foot Flexion Device - The invention relates to an ankle-foot flexion device that is configurable to provide both plantar flexion and dorsiflexion support. A leading loop and base loop are adapted to engage the foot and ankle and can be constructed of elastic material. Tension straps provide a pulling force between the base loop and a leg cuff. The tension straps are adjustable and can be positioned according to the needs of a particular user. | 2016-02-04 |
| 20160030223 | ANKLE FOOT ORTHOTIC JOINT - An improved AFO joint is described herein with improved stability and anti-rotational features. In particular, the AFO joint comprises a body portion with a medial beam for support and improved patient gait. Additionally, the AFO described herein comprises a tensioning member with high strength and a low profile for improved biomechanical effect. | 2016-02-04 |
| 20160030224 | DYNAMIC LUMBAR REALIGNMENT SYSTEM - A dynamic lumbar realignment system includes a compressive lower body garment that provides abdominal compression and a stabilizing strap that induces thigh rotation in order to produce a therapeutic effect. Pelvic tilt provided by the compressive lower body garment and thigh rotation provided by the stabilizing strap assist the user in maintaining proper posture. The stabilizing strap is arranged and oriented on the compressive lower body garment in a therapeutic orientation path that enables the stabilizing strap to exert a desired therapeutic effect on the user. The therapeutic orientation path is defined by a combination of a plurality of strap-supporting attachment points and a plurality of strap-guiding attachment points on the compressive lower body garment. Numerous variants of the dynamic lumbar realignment system are available to address various issues such as lumbar hyperlordosis and lumbar hypolordosis. | 2016-02-04 |
| 20160030225 | DEVICE FOR FIXING A TEST PERSON ON A STANDING SURFACE - The invention relates to a device for fixing a test person on a standing surface, wherein at least one rope is tensioned between a hip belt placed on the test person and a retaining plate arranged below the standing surface. | 2016-02-04 |
| 20160030226 | CATHETER ASSEMBLY WITH DEPLOYABLE COLLECTION CONTAINER - Catheter assemblies for draining urine from the urinary system of the user are disclosed herein. The catheter assemblies include an outer sleeve that houses the catheter tube and a deployable flexible container. The container is deployable through a slot in the sleeve wall and can be retracted back into the sleeve after use. | 2016-02-04 |
| 20160030227 | IMPLANT - An implant that has a tubular interior section for implantation into a patient, an exterior section connected to the interior section and an ingrowth member that includes a three-dimensional porous structure. The three-dimensional porous structure is typically located at the inner circumference of the interior section and has desirable properties to facilitate ingrowth of tissue. | 2016-02-04 |
| 20160030229 | METHOD AND SYSTEM FOR BREATHING MODULATION - A nasal breathing aid comprising the following components: a housing; facial engagement means attached thereto; at least two nostril pieces coupled to the housing. On the housing, there are at least two nasal inlets; at least one vent; and in the housing: a first passage and a second passage, each communicating an inlet with a vent, and fluid-isolated from each other, and restriction means configured to allow free flow of air through each passage from a vent to an inlet, and flow of air through the first passage independently restricted from flow of air through the second passage, from an inlet to a vent. | 2016-02-04 |
| 20160030230 | DEVICE FOR THE HINDRANCE OF SNORING AND OBSTRUCTIVE SLEEP APNEA - A head-wearable device is disclosed. The head-wearable device includes a headgear support structure, a band structure for securing the headgear support structure to the wearer's head, and a protrusion assembly affixed to the headgear superstructure for hindering the wearer's head from assuming a supine position during sleep. A method of sleeping is also disclosed. | 2016-02-04 |
| 20160030231 | DEVICE FOR REDUCING SNORING - A device for reducing snoring includes a ventilation tube having an air passageway therein and a first opening and a second opening at opposite ends of the air passageway, wherein a diameter of the first end is greater than that of the second opening, and a holding member connected to the ventilation tube at an end having the first opening. Put the device of the present invention in mouth may hold a normal shape of the upper respiratory tract while the user is sleeping and ventilate the air without obstruction while the user is breathing, so the user would not snore in sleep to improve the quality of sleep. | 2016-02-04 |
| 20160030232 | DENTAL RETAINER SYSTEM - Systems and methods for securing a person's upper jaw in place relative to the lower jaw. Included are dental mounts affixed to teeth on the upper and lower jaw as well as a support affixed between the mounts to hold the jaw in place. Some embodiments include an extended support having a substantially U-shaped portion for protecting teeth from injury. | 2016-02-04 |
| 20160030233 | APPARATUSES AND METHODS FOR COOLING A SURFACE - Methods and apparatuses for providing localized cooling of a surface are described. Localized cooling devices may include a thermal element configured to generate a temperature gradient in a cooling interface in contact with the surface. Temperature gradient may operate to facilitate conductive heat transfer from the surface, through the cooling interface, and out into the ambient environment. The thermal elements may include thermoelectric cooling elements (TECs), such as Peltier cooling elements. In some embodiments, the localized cooling devices may be configured to treat swelling associated with periorbital edema by providing convenient, efficient, and continuous cooling of the affected area. | 2016-02-04 |
| 20160030234 | DEVICES, SYSTEMS AND METHODS OF COOLING THE SKIN - According to some embodiments, a thermal conditioning system for selectively cooling skin of a subject comprises at least one thermal conditioning device comprising a first side and second side, the second side being generally opposite of the first side. In some embodiments, the system further comprises a heat sink positioned along the second side of the at least one thermal conditioning device, wherein the first side of the at least one thermal conditioning device is configured to be placed in contact with or in close proximity to a skin surface of the subject to selectively cool or heat the skin surface. | 2016-02-04 |
| 20160030235 | SLUSH GENERATION - Apparatus for generating, at a target ice/liquid ratio with a corresponding target temperature, a slush comprising frozen and non-frozen liquid comprises a flow path for recirculation of liquid therethrough, the flow path comprising a heat exchanger having a coolant inlet and a coolant outlet, the heat exchanger being configured for flow therethrough of coolant at a temperature below the target temperature, the apparatus being configured to vary the rate of coolant flow through the heat exchanger between a first rate and a second rate that is lower than the first rate. | 2016-02-04 |
| 20160030236 | COMPRESSION SEQUENCED THERMAL THERAPY SYSTEM - A sequential compression and temperature therapy blanket with a plurality of air chambers is disclosed. The air chambers are filled and released by a valve assembly that may be separate from or integrated within the blanket. The temperature therapy blanket includes a fluid bladder for delivering hot and/or cold therapy to a patient. The temperature therapy blanket may also include an air bladder for providing compression. | 2016-02-04 |
| 20160030237 | THERAPEUTIC TREATMENT PAD - A treatment pad for applying heat, cooling or an antiseptic fluid to a subject's body surface incorporates a heat transfer member or a wound treatment member that is adapted to be held in place by application of a vacuum pressure. The heat transfer member may comprise an electrical resistance wire arranged in a serpentine pattern within a housing or, alternatively, may comprise interconnected heat transmissive tubing through which either a heated or a cooled fluid may be made to pass. Alternatively, the pad may contain a gel that can be cooled in a refrigerator or heated in a microwave oven and held in place on the subject's body by application of a vacuum to the assembly. The wound treatment member may comprise a gaseous antiseptic delivery pad held in place on the patient's body by use of a vacuum. | 2016-02-04 |
| 20160030238 | CEREBRAL PROTECTION SYSTEM - A cerebral protection system generally includes an array of cold packs, an insulating cover, and optionally a set of trays. The cold pack contains two reactive materials separated by a rupturable membrane. When the first reactive material and the second reactive material are mixed, an endothermic reaction occurs. The system can be used to induce hypothermia in selected regions of the brain when used. | 2016-02-04 |
| 20160030239 | PUPIL EXPANDER - The purpose of the present invention is to provide a pupil expander capable of being safely arranged without damaging an iris and capable of maintaining a sufficiently expanded state of a pupil during ophthalmologic surgery such as cataract surgery. This pupil expander | 2016-02-04 |
| 20160030240 | MICROMANIPULATION SYSTEMS AND METHODS - A micromanipulation system includes a micromanipulator that includes a handpiece, and a micromanipulation tool that includes a tool shaft and is operatively connected to the handpiece. The micromanipulator further includes an actuator assembly connected to the micromanipulation tool to provide manual control of the micromanipulation tool, and a force sensing system comprising a force sensor attached to the tool shaft. The force sensing system is configured to provide an output signal that indicates a force imposed on the tool shaft. The micromanipulation system also includes a processor that is in communication with the force sensing system, and is configured to receive the output signal and compensate for forces due to actuation of the micromanipulation tool to determine a force due to interaction of the micromanipulation tool with a region of interest. The processor outputs an indication of at least one of a magnitude and a direction of the determined force. | 2016-02-04 |
| 20160030241 | OPTHALMIC DEVICE FOR CELL REMOVAL - In described embodiments, an ophthalmic device provides for cell removal. In one embodiment, the ophthalmic device is introduced into the eye to remove cells on the underside of the anterior capsular membrane and the posterior capsular surface that can grow and block vision in an eye following cataract surgery. The ophthalmic device includes a disk with either a cleaning edge or tacky substance, and is inserted via shaft, the shaft coupled directly to the disk and forming a cannula, or optionally coupled to the disk with a separate cannula there between. | 2016-02-04 |
| 20160030242 | Miniature Glaucoma Shunt - A glaucoma shunt ( | 2016-02-04 |
| 20160030243 | TECHNIQUE FOR LASER-CUTTING AN ENDOTHELIAL CORNEAL GRAFT - A method for preparing an endothelial corneal graft is provided. The method comprises: providing a donor cornea; irradiating the donor cornea from an endothelial side thereof with laser radiation to cause a photodisruption in tissue of the donor cornea at a focal point of the radiation; and moving the focal point of the radiation to form an endothelial graft in the donor cornea. By irradiating the donor cornea from the endothelial side thereof, instead of the epithelial side, to cut the endothelial graft, optical inhomogeneities which may develop after death in stromal tissue of the donor cornea leave the laser cutting process substantially unaffected. | 2016-02-04 |
