The invention relates to a prosthesis for implantation into a living body in the form of a magnetic artificial joint, in particular an artificial shoulder joint, comprising: a) a first prosthesis member comprising a socket member, b) a second prosthesis member comprising a head member, c) one of the socket member and the head member is at least partially composed as a permanent magnet and the other one of the socket member and the head member is at least partially composed of a magnetic material, or the socket member and the head member are both at least partially composed as a permanent magnet, d) the socket member comprises a recess on a surface side to be coupled with the head member, the recess comprising a concavely contoured contact surface, e) the head member comprises a projection on a surface side to be coupled with the socket member, the projection comprising a convexly contoured contact surface, f) the convexly contoured contact surface is adapted to the concavely contoured contact surface, such that the head member can be coupled in a rotatably jointed manner to the socket member in the nature of a ball/ball-socket joint, g) wherein the convexly contoured contact surface can perform a generally slip-fee rolling motion or a combined slipping and rolling motion on the concavely contoured contact surface in reaction to a change of an angle between the first and the second prosthesis member, and the convexly contoured contact surface can be shifted across the concavely contoured contact surface within a shifting area.

A joint replacement system for repairing an articular surface of a first bone of a joint includes an anchor portion and an implant portion. The anchor portion includes an anchor to be secured to the bone, and an anchor fixation head including a bone-facing surface (BFS) extending radially outward from the anchor and an implant facing surface (IFS) extending from a periphery of the BFS. The implant portion is formed from a material (e.g., CoCr) more dense than the material of the anchor portion (e.g., Ti) and includes a fixation cavity to receive at least a portion of the anchor fixation head (AFH), the fixation cavity includes an anchor facing surface (AFS) configured to form a frictional connection with the IFS, and a load bearing surface having a contour for articulating against a cooperating articulating surface of a second bone of the joint.

A method of implanting a prosthetic stemless shoulder implant may include making an incision into a patient's shoulder area of a patient and passing a cutting instrument through a rotator cuff interval of the patient. A central portion of the native humeral head may be resected and removed so that a central void remains. The same or another cutting instrument may be inserted through the rotator cuff interval and into the central void. Medial and lateral portions of the native humeral head adjacent the central void may be resected and removed. A base of a prosthesis may be implanted into a proximal portion of the humerus after passing the base through the rotator cuff interval, and two humeral head portions may be inserted through the rotator cuff interval and coupled to the base and to one another.

The present disclosure includes apparatuses, systems, and methods for vertebral disc repair. An example apparatus includes a first surface including a concave opening configured to receive an artificial disc, a second surface, and an aperture extending through the first surface and the second surface, wherein the aperture is configured to receive a bone screw.

Provided for herein, in several embodiments are implants and methods of using same to repair damaged or defective soft tissue. In several embodiments, the soft tissue comprises cartilage within a joint space. In several embodiments, the implants provided for comprise a stimulating region and an anchoring region. In several embodiments, the implants are spherical. A discontinuity between a surface of the implant and the surrounding cartilage advantageously facilitates implant placement and stimulation of generation of fibrous tissue, and subsequently new cartilage.

Implants, device, systems and methods for replacing an articulation surface in a joint, for example, a glenoid implant with an articular surface and an opposing bone contacting surface having a ring and post extending therefrom that respectively mechanically connect with cortical bone and cancellous bone of a glenoid. Methods for implanting the glenoid implant are also disclosed.

The present disclosure provides an iliac prosthesis, comprising: a prosthesis main body, the prosthesis main body including a first end portion contacted and matched with a sacrum and a second end portion contacted and matched with an acetabulum, a first screw hole being formed in the first end portion, a first screw seat being arranged in the first screw hole, the screw-rod structure including a connecting seat and a rod body, the connecting seat being connected with the prosthesis main body, and the rod body being fixed on the connecting seat; and an anti-dropping mechanism, the anti-dropping mechanism being arranged between the prosthesis main body and the connecting seat in a clamping manner. The technical solutions of the present disclosure can effectively solve the problems of unreliable supporting and easy fatigue break of the screw-rod system in the related technology.

A customized artificial temporomandibular joint unit according to an embodiment of the present disclosure includes a first plate provided along a lower line of a lower jawbone forming a temporomandibular joint and having an insertion groove that is outwardly open, a second plate provided at a temporal bone forming the temporomandibular joint together with the lower jawbone, and a main prothesis detachably combined to the first plate without a separate fastening device by being forcibly fit into the insertion groove while approaching the first plate, and arranged in a customized manner at a facing surface location facing the second plate.

A hip/shoulder prosthesis includes: a head component; a metaphyseal component; a diaphyseal nail, and a locking device. The head component includes: a front face and rear face; with a bore, and first and second shaped recesses in the rear face. The metaphyseal component includes: a central transverse aperture at an angle to the metaphyseal component's axis; a first end configured for threaded engagement within the bore of the head component; and a longitudinal hole that begins at the second end, transects the transverse aperture and reaches the first end, to receive the locking device. The diaphyseal nail is inserted in the femoral or humeral canal, and includes: fastening apertures that receive corresponding screws for fastening the diaphyseal nail to the femur or humerus; a portion configured to be received within, and engage, the transverse aperture of the metaphyseal component, and a transverse hole configured to receive the locking device.

The strength of bone implant attached to a bone is improved by using hybrid inserts which have stems and wings having bone ingrowth surface features and caps having outer surfaces of cured polymethyl methacrylate (PMMA). The stems and wings of the hybrid inserts are inserted into living bone and the bone implant is attached to the hybrid inserts with PMMA cement. Over time, the bone grows into the bone ingrowth surface features. The bone ingrowth strengthens the bonding of the hybrid inserts and the bone implant with the bone over time. The hybrid inserts increase the shear, tensile and torque strength of the bone implants. Bone inserts that do not have ingrowth surface features loosen over time.