Prosthetic devices allow for full articulation of the joint, while absorbing impact of the components during normal use that will reduce wear on the device components and prolong life. The device may include a bone implantable component and a bearing component having an articulation surface that is sized and shaped to substantially mate with at least a portion of the bone implantable component and a damping mechanism that includes a contact member disposed at least primarily inside a cavity; a biasing member biasing the contact member toward an upper aperture of the cavity and means for capturing the contact member within the cavity.

A lattice or solid structure for a medical device includes a first layer of first filaments discretely formed from at least one medical-grade silicone material. The first filaments are arranged in a predetermined pattern and may be directly adjacent to one another or spaced apart. Additional layers of filaments may be provided adjacent to the first layer, and chemically bonded thereto to form an integrated structure that is without interruption or with interstices therebetween.

A device and method for managing a plurality of groups of socks where the device includes a plurality of pouches attached to one another and a patient education and compliance tool. Each group has at least one sock. Socks of each of the groups have different characteristics from one another. The groups of socks are adapted for use between a limb of a patent and a socket of a prosthetic device. Each pouch is adapted for securing at least one sock from a group. The method includes sorting the plurality of groups of socks according to the characteristic, associating each pouch with a respective one of the groups, and securing each group of socks within an associated pouch.

A seal component for a prosthetic liner comprises a base portion located at a distal portion of the seal component and anchored circumferentially to an exterior surface of the liner; a seal wall arranged to flexibly and movably extend relative to a body of the liner; at least two seal rings radially and outwardly extending from the seal wall; and an outwardly pitched portion at the distal end of the seal component and extends obliquely away from the base portion relative to the axis of the seal component, and an inwardly pitched portion at the proximal end of the seal component and extends obliquely toward the axis of the seal component, the at least two seal rings are located between the outwardly and inwardly pitched portions.

A method for reducing motion of a skeletal structure in a limb towards a wall of an interface is described. The interface comprises a plurality of compression areas that are longitudinally-shaped and oriented longitudinally along the length of limb. The method comprises selecting, during a process of creating the interface, a compression level for the compression areas that compresses soft tissue against the skeletal structure. The method also comprises donning the interface over the limb to apply a plurality of compressive forces that is sufficient to aid in suspension of the interface on the limb and reduce motion of the skeletal structure toward a wall of the interface.

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 lattice or solid structure for a medical device includes a first layer of first filaments discretely formed from at least one medical-grade silicone material. The first filaments are arranged in a predetermined pattern and may be directly adjacent to one another or spaced apart. Additional layers of filaments may be provided adjacent to the first layer, and chemically bonded thereto to form an integrated structure that is without interruption or with interstices therebetween.

An adjustable prosthesis system for a residual limb includes: an adjustable outer shell surrounding the residual limb having a plurality of overlapping flaps, a top opening along a top edge extending around the outer shell, a bottom having a bottom edge opposite the top edge and extending around the bottom, a first side, and a second side having an adjustable width, and a plurality of adjustable overlapping side ends, some of which overlap and some do not, extending from the top edge to the bottom edge; a base adjacent the bottom of the outer shell and connected to it; and a closure component attached to the outer shell to compress the residual limb. Tightening the closure component applies a pulling force to at least one of the first side and the second side, thereby causing a reduction in width of a discontinuity and increased overlap of the side ends.

A prosthetic interface includes a body portion having an open proximal end and a closed distal end including a distal cup. The body portion includes a membrane component having a flexible configuration defining an internal flow space extending along a length of the membrane component between an inner side arranged to face a skin surface of a residual limb and an outer side arranged to face away from the skin surface. At least one material coating is selectively applied to the membrane component that interacts with at least one of the membrane component and the distal cup to define at least one breathable region along the inner side that allows fluid flow between the internal flow space and the residual limb, and at least one impermeable region along the outer side that allows for vacuum suspension between the prosthetic interface and a prosthetic socket.

A liner is arranged for use in prosthetic and orthopedic devices. The liner defines first and second end portions, and inner and outer surfaces. The liner includes an inner layer having a frictional component and forms at least part of the periphery of the inner liner surface. The inner layer defines a plurality of apertures. A porous element is in communication with the inner liner surface and is connected to the inner layer such that the apertures permit a transfer of air from the inner surface to the porous element. A base layer adjoins the porous element and extends between the first and second end portions of the liner.