Abstract: A digit prosthesis assembly is described. Embodiments of the digit prosthesis assembly include, but are not limited to, an attachment assembly, a thumb assembly, one or more finger assemblies, a pinky finger assembly, a palm engagement assembly, and combinations thereof.

Abstract: A seal member for use with a replacement heart valve implant may include a tubular polymeric seal element configured to be disposed on an outer surface of a replacement heart valve implant, the tubular polymeric seal element defining a central longitudinal axis; and a reinforcement strip fixedly attached to the tubular polymeric seal element proximate a first end of the tubular polymeric seal element, the reinforcement strip extending circumferentially around the central longitudinal axis. The reinforcement strip may include a radiopaque element extending circumferentially around the central longitudinal axis.

Abstract: Through observation it has been determined that deployment of delivery sleeves may result in one or more portions of the deliver), sleeve extending beyond an end of the endoluminal device resulting in an overhang of material. The overhang may affect blood flow through the endoprosthesis or otherwise impact performance, including facilitating unwanted tissue growth. Various inventive concepts are provided for addressing (reducing or removing) constraining sheath overhang.

Abstract: An apparatus for protecting a post-amputation residuum comprises a shell defining a hollow interior cavity adapted for receiving and covering a distal portion of the residuum. The shell has an opening into the cavity at the distal end. A first and a second plurality of circumferentially spaced longitudinal slits extend from the proximal end and the distal end, respectively. A proximal portion of a compression sleeve is disposed over at least a portion of the residuum. A free distal portion of the sleeve extends through the opening in the shell and everts upon application of a longitudinal force to the distal portion of the sleeve in a proximal direction for folding over and covering the shell. The distal portion of the sleeve extends proximally of the shell to a position at least partially along the proximal portion of the sleeve for compressing the shell inwardly toward the residuum.

Abstract: An insert (240) arranged and configured for use in a dual mobility acetabular implant (100) is disclosed. The insert includes a plurality of chamfers (260, 262, 264) arranged and configured to contact the femoral neck (172) and/or head (170) of a femoral implant (175). The insert includes a plurality of chamfers such as, for example, two or three chamfers to define a plurality of differently arranged contact surfaces for contacting the femoral component to accommodate a variety of different femoral component configurations and/or impingement conditions in order to reduce contact stress between the insert and the femoral component.

Abstract: The invention relates to a prosthetic foot comprising a main body (10), a proximal connection device (15) for connecting the prosthetic foot (1) to a further prosthesis component, and a foot-front component (12) which is pivotally mounted on the main body (10) and which is associated with a resistance device (20), which resistance device retards plantar flexion of the foot-front component (12), wherein the foot-front component (12) is mounted on the main body (10) via at least one resilient component (30, 31, 32) which moves the foot-front component (12) back into a starting position after a deflection.

Abstract: A dilation device for an intra-body lumen, for example, a urethra partially occluded by an enlarged prostate in the form of a resilient curved body configured to be implanted in a cut around the lumen, and a method for dilating such a lumen by implanting a dilation device in a cut around the outside of the lumen. Also, a deployment system including a delivery device for the implant, and a device for dilating the lumen before and while the cut is being made, and a method of using the implant and the deployment system. The implant may be formed of a strip or a coiled wire. The cut may be performed in part by the implant. The cut may be performed by a sharp edge, and/or by application of electrical current to the area being cut, or by a piezoelectric transducer.

Abstract: The invention relates to an orthopedic joint device having an upper part and a lower part which is hinged about a pivot axis to said upper part, having a flexion moment-controlled retainer device that is positioned between the upper part and the lower part, blocks a flexion and releases the flexion when a predefined flexion moment is exceeded, wherein a control element is associated with the retainer device and is coupled to a delaying element.

Abstract: A hydraulic actuator for orthotics or prosthetics, comprising a control element with a housing, in which a cylinder is arranged, in which a piston is mounted so as to be movable and divides the cylinder into a flexion chamber and an extension chamber, a fluidic connection is arranged between the flexion chamber and the extension chamber, and in each of said chambers there is arranged a control valve for influencing the extension movement or flexion movement, a motorised pump being arranged in the fluidic connection, with the hydraulic fluid being conducted from one chamber to the pump through at least one control valve in an intake-side connection line, and a check valve being arranged in a delivery-side connection line from the pump to the other chamber and blocking a return flow of the pumped medium from this chamber to the pump against the conveying direction of the pump.

Abstract: Certain aspects of the present disclosure provide a flexible scaffold implant comprising a plurality of layered structures, the plurality of layered structures comprising: a first layered structure having a three-dimensional (3D) shape and formed from a bioresorbable material, and a second layered structure conforming to the corresponding 3D shape of the first layered structure and formed from the bioresorbable material. The first layered structure is arranged in proximity to the second layered structure. The first layered structure is configured to dissolve for resorption at a different rate than the second layered structure based on design elements of the first layered structure and the second layered structure. The plurality of layered structures are flexible.

Abstract: A prosthetic heart valve can include a frame defining a central longitudinal axis and a plurality of leaflets. Each leaflet can include: a leaflet free edge, a first leaflet side forming a first leaflet side line of attachment along the frame, a second leaflet side forming a second leaflet side line of attachment along the frame, and a leaflet base forming a leaflet base line of attachment along the frame from an end of the first leaflet side line of attachment to an end of the second leaflet side line of attachment. The first leaflet side line of attachment can form a continuous attachment of the first leaflet side to the frame along an entire extent of the first leaflet side. The second leaflet side line of attachment can form a continuous attachment of the second leaflet side to the frame along an entire extent of the second leaflet side.

Abstract: An illustrative prosthesis and orthosis testing system includes a platform that receives a prosthesis or orthosis. A motor or a weight are configured to apply a load to the prosthesis or orthosis, and one or more load cells are configured to measure a magnitude of the load on the prosthesis or orthosis. The system also includes one or more encoders configured to measure one or more positions and one or more orientations of the prosthesis or orthosis in response to the applied load.

Abstract: A prosthetic system with a prosthesis, which has two prosthetic parts that are pivotally connected together about a joint axis via a prosthetic joint with a joint upper part and with a joint lower part, and a cover element, which at least partly covers a gap between the two prosthetic parts or between one prosthetic part and the joint lower part. The cover element is pivotally mounted about a pivot axis on one prosthetic part, a component of a cosmetic prosthetic element, said component being secured to one prosthetic part or one joint part or the prosthetic joint and is coupled to the joint upper part of the prosthetic joint via at least one coupling element in a form- and/or force-fitting manner such that a pivotal movement of the prosthetic parts about the joint axis leads to a simultaneous pivotal movement of the cover element about the pivot axis.

Abstract: Embodiments include a prosthetic thumb device that includes a track configured to attach to a prosthetic socket, a carriage, and a locking mechanism. The carriage can include a first component that couples to the track such that the carriage is operable to move along the track, and a second component that is configured to couple with a prosthetic digit and operable to rotate with respect to the first component. The locking mechanism can be coupled to the carriage and configured such that, in a first state, it prevents the carriage from moving along the track in a first direction and, in a second state, it allows the carriage to move along the track in the first direction. Embodiments can also include the track having a curved profile, and the carriage is operable to move along the curved profile of the track.

Abstract: The invention relates to prosthesis for treating pulmonary fibrosis, in particular, idiopathic pulmonary fibrosis (IPF), and a method for treating pulmonary fibrosis, in particular, idiopathic pulmonary fibrosis (IPF).

Abstract: A prosthetic hand with a chassis (20) and at least one base element (10) for fastening a prosthetic finger to the chassis (20), wherein a longitudinal guide for the base element (10) is arranged or formed on the chassis (20), the base element (10) being mounted in said longitudinal guide, wherein the longitudinal guide blocks two translational degrees of freedom and a clamping element (30) is assigned to the longitudinal guide, said clamping element being displaceably mounted in or on the chassis (20) or the base element (10) between a locking position and an unlocking position and effecting a blocking of the third translational degree of freedom in the locking position.

Abstract: The present disclosure discloses an ankle prosthesis containing zirconium-niobium alloy on oxidation layer and a preparation method thereof, the preparation method comprises: using zirconium-niobium alloy powder as a raw material, conducting a 3D printing for one-piece molding to obtain an intermediate products of the talus part and tibial part, and performing Sinter-HIP, cryogenic cooling and surface oxidation to obtain talus part and tibial part. The talus part is connected with the tibial part in a sliding mode; a bone trabeculae is respectively arranged on the lower surface of the talus body and the outer surfaces of the two first fixations, and on the upper surface of the tibial body and the outer surfaces of the two second fixations as well, so as to improve bone ingrowth.

Abstract: A prosthetic foot includes a spring component and a sole component. The spring component comprises two or more stacked beam elements, each beam element including, along the length of the respective beam element, a first portion and a second portion, and the second portion of the beam element includes an extent with a length-varying width. The respective beam elements are fixed to each other and to the sole component proximate the heel portion of the sole component or the toe portion of the sole component at the first portions of the respective beam elements to form a fixed end of a cantilevered composite beam. The second portions of the respective beam elements are laterally movable with respect to each other when the spring component deflects.

Abstract: A prosthetic liner includes a textile cover having at least first and second regions having different elongation from one another. The first region is in a prestretched configuration in at least one orientation relative to an axis of the prosthetic liner and locked in the prestretched configuration according to a layer of elastomeric material located along a surface of the textile cover.

Abstract: Techniques are provided for using machine learning methods to predict user preferences with respect to robotic assistive prostheses and/or custom tune the robotic assistive prostheses for individual users based on the predicted user preferences. A training biomechanical dataset, including historical biomechanical sensor data for a robotic assistive prosthetic device operating using a plurality of tuning settings at a plurality of speeds, and a training user preference dataset including historical user tuning preference data for the robotic assistive prosthetic device for each respective tuning setting and speed, are generated. A machine learning model is trained using the training biomechanical dataset and the training user preference dataset.