Abstract: A prosthetic device includes a first material and a second material that surrounds a least a portion of the perimeter of the first material. The first material and the second material have a resting shape that is configured to fit a body part on which the prosthetic devices is to be implanted. The second material is deformable to fit the prosthetic device through an opening of the subject smaller than the resting shape to reach the body part. A prosthetic device can be produced by obtaining image data corresponding to a body part of the subject, generating and refining one or more models of a body part based on the image data, and producing the prosthetic device as a three-dimensional print of the refined model.

Abstract: A prosthetic knee having a passive knee locking mechanism that uses the same four-bar mechanics found in a natural knee. The flexible four-bar mechanism guides the motion of the knee, aids in the return of the knee from full flexion to extension, and connects a femoral gear to a tibial gear. The gears have a circular radius and are connected using parallel links to keep the femur and tibia together when the knee is active. The knee stays locked throughout the stance phase. At toe off, no weight is applied on the prosthetic knee allowing the knee to flex. The flexible links are stretched, thereby increasing the stiffness in the springs, and at terminal swing phase, moments before heel strike, the flexible links in the four-bar mechanism snap back to the extended/locking position and lockout once the user applies his/her weight on the knee.

Abstract: An aortic prosthesis for the treatment of abdominal aortic aneurysms, wherein the prosthesis is implanted intraluminally and comprises a main body having a generally cylindrical shape with an upper portion intended to be secured firmly above the renal arteries through an anchoring means, a lower portion freely moving at a position within the aneurysm and above the iliac arteries, and an intermediate portion arranged between the upper and lower portions, and the main body comprising a flexible fabric of woven material having a very loose weave in the upper portion so as to allow fluid communication between the interior of the prosthesis and the renal arteries, an intermediate weave in the intermediate portion and a tight weave in the lower portion of the main body.

Abstract: An ophthalmic device includes an optic including an optic axis and a haptic structure coupled with the optic. The haptic structure includes an inner ring comprising a plurality of hinges such that portions of the inner ring reside at different radii from the optic axis. The haptic structure further includes a first loop extending from the inner ring and having two points of connection to the inner ring and a second loop extending from the inner ring and having two points of connection to the inner ring. The second loop is oriented opposite the first loop.

Abstract: A two-part joint replacement device for replacing damaged soft joint tissue, such as a meniscus or cartilage tissue. In one form, the device may include a free floating soft joint tissue replacement component comprising a first tissue-interface surface shaped to engage a first anatomical (bone and/or cartilage) structure of a joint having damaged soft tissue. The device may also include a free floating rigid base component comprising a second tissue-interface surface shaped to engage a second anatomical (bone and/or cartilage) structure of the joint. The free floating soft joint tissue replacement component may be shaped to slidably interface with the rigid base component. In another form, the free floating soft joint tissue replacement component and the rigid base component are fixed together.

Abstract: A device for ligament reconstruction includes an elongated body and a hook or loop at each end for receiving a ligament reconstruction member such as an allograft or autograft tendon. The ligament reconstruction member is positioned within a hole that is drilled into a bone, or which is provided within a prosthetic joint. A central portion of a ligament reconstruction member is passed through each end of the device. The ends of the ligament reconstruction members are then fastened to the opposing bone forming the joint.

Abstract: An adapter module (2) configured to be attached, by a predetermined number of screws (4), to a socket member (6) of a prosthetic sleeve (8), into which sleeve (8) an amputation stump of a prosthesis user is to be inserted. The adapter module (2) comprises a module body (10) provided with a washer space (12) structured to provide room for a disc-shaped connection washer (14), the washer space (12) has an extension to provide for movement of the connection washer (14) within a plane essentially perpendicular to a longitudinal axis A of said prosthetic sleeve (8) prior the connection washer (14) is fixated in a determined position. The connection washer (14) is provided with a through-going first opening (16) structured to receive a washer attachment screw (18) such that the screw essentially extends along said longitudinal axis A. The through-going first opening (16) is preferably positioned off-centered of the washer (14) in order to maximize movement of the washer in all directions within the plane.

Abstract: An expandable stent comprises a cylindrical wall made up of lattice members connected to each other, at least one first arm and at least one second arm. The first arm comprises: a first non-linear member that is connected at each of its axial ends to a lattice member at respective first junctions; a second non-linear member connected at each axial end to a lattice member; and at least one bridge member extending between the first member and the second member. The second arm comprises: a first non-linear member that is connected at each of its axial ends to a lattice member; a second non-linear member connected at each axial end to a lattice member; and at least one bridge member extending between the first member and the second member. The second member of the first arm is generally U-shaped, extending from its axial ends towards: (i) a first axial end of the stent; and (ii) towards the bridge of the first arm.

Abstract: An eye enlargement implant and a method of performing a cosmetic procedure for the beauty of eyes, which is capable of being inserted into the eyes so as to make the eye look crisper and bigger, and being removed when it is not necessary without causing eye inflammation and without having to be replaced, the implant including a ring-shaped body which is inserted between a sclera and a conjunctiva of an eyeball having an inner diameter portion having at least a size enough to surround an outer periphery of the cornea, and an outer diameter portion having a width size of 0.8 to 1.2 mm so as to cover a white portion and having a maximum thickness of 0.05 to 0.20 mm at the center portion, where the ring-shaped body has flexibility and a predetermined color which is similar to that of the iris.

Abstract: A subtalar implant for arthroereisis of the talocalcaneal joint. The implant is intended to be inserted into the talocalcaneal joint via its lateral orifice and has an oblong shape that extends longitudinally along an axis of insertion of the implant. The implant includes: a head with the shape of a cone of revolution centred on the axis of insertion; an anchoring thread; and a rod having the shape of a cylinder of revolution. The rod has, on its surface, the anchoring thread and being configured to be inserted up to the axis of rotation of the talocalcaneal joint. The head has, on its radially outer surface, a retaining element for retaining the implant in rotation about the axis of insertion, the retaining element exerting retention against a colonising tissue.

Abstract: A subcutaneous sling for neck lift surgery. The sling comprises a sling body, shaped to fit in a submental triangle of a patient undergoing neck lift surgery, comprising a narrow anterior edge for anchoring near the chin of the patient. The sling comprises two lateral sling extensions, each coupled to a respective side edge of two sides of the sling body, each projecting away from the center of the sling body in a posterior lateral orientation of between 45 and 90 degrees from the anterior-posterior axis, and curved slightly towards the narrow anterior edge to fit the submandibular triangle and extend to near each ear of the patient. The sling body is at least 4 centimeters long in the anterior-posterior dimension, and the ends of the two lateral sling extensions are at least 14 centimeters distant from each other.

Abstract: The present disclosure relates to a powered exoskeleton. The powered exoskeleton includes a leg connection rod and a stabilizing structure. The stabilizing structure is mounted on the leg connection rod. The stabilizing structure is switched between a folded state and an unfolded state in such a manner that the stabilizing structure is folded on the leg connection rod when the stabilizing structure is in the folded state, and the stabilizing structure is suitable for being in contact with the ground and supports the leg connection rod in a tilted upward direction when the stabilizing structure is in the unfolded state.