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 method for making a mould of an amputation stump, in which the amputation stump is inserted into a liner of a moulding aid, the liner having a longitudinal direction and a circumference, and the liner having an expansion coupling such that when the liner is extended in the longitudinal direction, this necessarily results in a reduction of the circumference.

Prosthetic socket sealing systems and methods of use. Embodiments of the present invention include various combinations of sealing elements that are associated with a rigid prosthetic socket and act to seal the socket interior against air intrusion or escape via the open proximal end thereof. The socket interior may thus be evacuated for purposes of vacuum suspension or otherwise.

A system for additive manufacturing a medical device, the system comprising a first dispensing system, a second dispensing system, a deposition apparatus, and a deposition substrate on a surface of which the deposition apparatus is configured to deposit at least one elastomeric material into a filament. The deposition apparatus receives the at least one elastomeric material from the first and second dispensing systems in proportions effecting a desired property in the medical device. The deposition apparatus may comprise heating and/or cooling elements, a sonic vibration module, and/or a pneumatic suck-back valve. The deposition substrate may have a configuration corresponding to a desired shape of the medical device and is configured to rotate and/or translate relative to the deposition apparatus. The system comprises a controller configured to control the deposition.

A single socket adjustable prosthetic system having a first shell with an extended surface configured to fit against a first side of an amputee's limb, the surface terminating at a base; a second shell configured to fit against a second side of the amputee's limb; an articulated hinge having a first member, a middle member, and a second member, the first member having a first plate connected to a second plate at an angle to each other, with the second plate hingedly connected to a first end of the middle member and the second member hingedly attached at a second end of the middle member, the first plate removably connected to the base and the second member of the articulated hinge attached to the second shell; a space between the first shell and the second shell, to be varied to hold, and accommodate the amputee's limb.

A multi-component frame includes a first component made from a rigid structural material and a second component connected to at least an end portion the first component. The first component is constructed from a metal or metal alloy, and the second component is constructed from a material different from the first component. The first and second components form at least part of a length of the multi-component frame.

A technology is described for determining an intended movement from neuromuscular signals. An example method (800) includes receiving electromyography (EMG) data corresponding to single-ended channels of an electrode array (810), where EMG signals are detected by electrodes comprising the single-ended channels of the electrode array and the EMG signals are converted to the EMG data. Determining differential channel pairs for the single-ended channels of the electrode array (820) and extracting feature data from the EMG data of the differential channel pairs (830). Thereafter a feature data set is selected from the feature data of the differential channel pairs (840) and the feature data set is input to a decode model configured to correlate the feature data set to an intended movement (850). Decode output is received from the decode model indicating the intended movement (860) and the decode output is provided to a device (870).

The invention relates to an enveloping body for at least partially enveloping a limb, having an enclosed volume and a connection for supplying and removing fluid to the volume or from the volume, wherein the enveloping body forms an inner circumference and an outer circumference; on the enveloping body reinforcement elements are arranged that are designed to be brought into contact as a result of the removal of fluid from the volume or to increase their contact with one another as a result of the removal of liquid.

A suspension liner has a liner body portion, a textile material, and a plurality of seals formed along a length of the suspension liner toward a closed distal end and protruding circumferentially about a liner profile. Each seal has a same shape including a peak having a rounded profile and a width narrowing toward the peak and defines a sealing surface arranged to form a secure interface with an interior wall of the socket that retains the suspension liner within the prosthetic socket. The textile material is located intermediate interior and exterior surfaces of the suspension liner that formed of one or more silicone materials in the area of the seals and the textile material defines the exterior surface of the suspension liner proximal and distal to the seals.

A prosthetic liner for use with a prosthetic socket that has a thermoplastic elastomeric (TPE) layer that is in contact with the amputee's residual limb. The TPE layer is not uniform in thickness but has ridges to extend circumferentially around the TPE layer. A fabric layer covers the outer surface of the TPE layer conforming to the ridges and is used as a substrate to form a mechanical bond to an outer seal layer. The outer seal layer is formed by applying an uncured material to the fabric around the ridges thereby creating an air tight boundary layer when inserted into a socket. When vacuum is applied the air is evacuated from the volume below the seal layer.