An adjustable socket system includes a socket frame having a proximal area, a distal area opposite the proximal area, a first component arranged along a first side of the socket system, and a second component arranged along a second side of the socket system. The first component is connected to the second component. A tubular insert is arranged on an interior of at least the proximal area of the socket frame. The tubular insert forms an interior surface of the socket system. At least one tensioning element operatively connects the tubular insert to the first and/or second components. At least one tensioner is attached to the at least one tensioning element that selectively tensions the tensioning element to adjust a circumference of at least one area of the socket system.

A prosthetic knee includes a housing, a chassis, and a brake member pivotally connected to the housing at a first location point and to the chassis at a second location point. A knee shaft extends through the brake member and is secured within a cavity defined by the housing. An extension assist system includes a biasing mechanism located inside of the chassis and an extension assist link. The extension assist link includes a body portion operatively connected to the biasing mechanism and a pair of arm portions situated in at least one slot defined by the knee shaft. The arm portions are pivotally connected to the knee shaft at a third location point located a distance from the first location point.

A prosthetic device having a proximal interphalangeal joint (PIP) and a metacarpophalangeal joint (MCP), comprising a first prosthetic digit comprising one or more first phalanges and a four-bar linkage to operatively couple the PIP joint to the MCP joint, a first engagement portion positioned on one of the first phalanges, the first engagement portion comprising a locking linkage extending along the phalange, the locking linkage being part of the four-bar linkage, and a first stopping portion comprising a stopping element configured to be positioned above the locking linkage, wherein the locking linkage is capable of engaging with the stopping element by passing the one of the first phalanges in which the locking linkage is positioned through a mechanical singularity to lock the first prosthetic digit such that each of the one or more phalanges is in a position of flexion in response to a force applied to the first prosthetic digit.

A method for producing a three-dimensional, multi-cell object, in which polymerized structures are produced in layers by the irradiation of light radiation. To this end, use is made of photopolymerizable liquids which at least partly comprise biological cells. The invention also relates to a device for carrying out such a method and to the use of this device for producing an artificial organ.

A variable gain impedance controller for use in a control system for controlling a motorized prosthetic or orthotic apparatus provided with a joint The controller comprises a sensor input for receiving a signal indicative of an interaction between the apparatus and the ground, a torque sensor input for receiving a signal indicative of the torque at the joint and a variable gain scheduler in communication with the sensor input so as to receive data therefrom thereby providing a variable torque gain. The variable gain impedance controller adjusts its control on the apparatus based on the variable torque gain and the indicated torque so as to a) increase the joint resistance to motion when the signal received from the sensor input indicates an interaction between the apparatus and the ground and b) decrease the joint resistance to motion when the signal received from the sensor input indicates an absence of interaction between the apparatus and the ground.

A prosthetic device is configurable between a predetermined shape configuration and a contracted configuration. The prosthetic device includes a resilient body having the predetermined shape configuration and defining a first surface and a second surface opposed to the first surface and separated by a wall thickness. An adjustment device is connected to the resilient body, and at least one elongate element engages at least one of the first and second surfaces and has a first end received by the adjustment device such that the adjustment device is arranged to regulate tension in the at least one elongate element. Tensioning of the at least one elongate element by the adjustment device urges the resilient body to collapse or compress into the contracted configuration, wherein release of tension of the at least one elongate element allows the resilient body to revert to the predetermined shape configuration.

A prosthetic device is configurable between a predetermined shape configuration and a contracted configuration. The prosthetic device includes a resilient body having the predetermined shape configuration and defining a first surface and a second surface opposed to the first surface and separated by a wall thickness. An adjustment device is connected to the resilient body, and at least one elongate element engages at least one of the first and second surfaces and has a first end received by the adjustment device such that the adjustment device is arranged to regulate tension in the at least one elongate element. Tensioning of the at least one elongate element by the adjustment device urges the resilient body to collapse or compress into the contracted configuration, wherein release of tension of the at least one elongate element allows the resilient body to revert to the predetermined shape configuration.

A pre-operative planning and manufacturing method for orthopedic surgery includes obtaining pre-operative medical image data representing a joint portion of a patient. The method also includes constructing a three-dimensional digital model of the joint portion and manufacturing a patient-specific alignment guide for the joint portion from the three-dimensional digital model of the joint portion when the image data is sufficient to construct the three-dimensional digital model of the joint portion. The patient-specific alignment guide has a three-dimensional patient-specific surface pre-operatively configured to nest and closely conform to a corresponding surface of the joint portion of the patient in only one position relative to the joint portion. The method further includes determining, from the image data, a size of a non-custom implant to be implanted in the patient and assembling a surgical kit including the non-custom implant when there is insufficient image data to construct the patient-specific alignment guide therefrom.

A prosthetic device. The prosthetic device may include a flexure cut and/or a sensor to detect movement in accordance with a degree of movement. In an embodiment, the sensor may be disposed within the flexure cut. Other embodiments include at least one wire configured to connect a sensor located in a distal portion to a proximal portion, while annularly traversing a joint.

A prosthetic device. The prosthetic device may include a flexure cut and/or a sensor to detect movement in accordance with a degree of movement. In an embodiment, the sensor may be disposed within the flexure cut. Other embodiments include at least one wire configured to connect a sensor located in a distal portion to a proximal portion, while annularly traversing a joint.