A hemi-arthroplasty bone joint implant has a first part (120) with a stem (111) tor intramedullary implanting into a metacarpal, and a second part (110) to engage the trapezium is a translational manner, a hemi-arthroplasty articulating coupling (121). This allows multi-axial motion with translational movement of the second part over the trapezium and rotation of the first part (110) about the articulating coupling (121, 103). There is also a converter to convert the implant to a toral arthroplasty implant in situ during revision surgery. The second part (110) and the hemi-arthroplasty coupling (100, 123, 121) are removable in situ during revision surgery. The first part (120) has an engagement threaded socket (117) for, after removal of the second part and the hemi-arthroplasty coupling, engaging the replacement coupling (200) and allowing mutual articulation of the first (120) and replacement parts (220). This forms a total arthroplasty joint implant.

An implant device is provided that is configured for implantation at multiple locations between adjacent vertebrae. The implant device comprises an implant body, a first portion of the implant body, and a second portion of the implant body adjustably interconnected with the first portion. The implant body has a compact orientation and an extended orientation to allow the implant body to be shifted from one orientation to the other orientation for being positioned in any one of areas between the spinous processes of the adjacent vertebrae, between laminar regions of the adjacent vertebrae, spanning an opening in the annulus between the adjacent vertebrae, and in the intervertebral space between the adjacent vertebrae.

A joint implant assembly including a spherical shaped component adapted to securing to an end of a first joint defining bone and a recess shaped component adapted to securing to an end of a second joint defining bone. Each of the components establishes an opposing wear surface, at which microscopic sized particles build up over time resulting from prolonged use of the joint. At least one of the spherical and recess shaped components exhibits a plurality of interior entrapment chambers, each of which including a narrow-most entranceway location communicating with the wear surface. The entrapment chambers further exhibit outwardly widening capture profiles extending within the associated component for securing volumes of the microscopic particles away from a zone defined between the wear surfaces.

Techniques for implantable orthopedic pain management devices are disclosed, including incising an opening in a synovial capsule substantially surrounding a joint, using a first tool to form an enlarged opening in the synovial capsule, determining whether to modify the joint, the joint being modified using a second tool if a bone structure coupled to one or more bones is found within the joint and the bone structure is configured to limit articulation of the one or more bones when an implantable device is inserted into the synovial capsule and the joint, and inserting the implantable device into the synovial capsule through the enlarged opening, the implantable device being inserted into the joint using a third tool.

Disclosed are a method for limiting diffusion of wear debris of an in vivo implant and an in vivo implant apparatus with a function of limiting wear debris. An elastomer seal is arranged at a wearing part between implant components that can move relatively and generate wear, such that an outlet for wear debris of the implant is always sealed within a sealing area formed by the seal and the implant components, thereby preventing the wear debris from diffusing outwards. The elastomer seal includes at least one flexible buffer part for reducing or completely offsetting relative motion between the implant components, thereby further reducing wear of a sealing part of the elastomer seal due to the relative motion between the parts. The seal is tightly attached to in vivo implant components, and the in vivo implant is smaller than a force for driving the components to generate relative motion.

Disclosed is a method for limiting diffusion of wear debris of an in vivo implant and an in vivo implant apparatus with a function of limiting wear debris. According to the present invention, an elastomer seal is arranged at a wearing part between implant components that can move relatively and generate wear, such that an outlet for wear debris of the implant is always sealed within a sealing area formed by the seal and the implant components, thereby preventing the wear debris from diffusing outwards. The elastomer seal includes at least one flexible buffer part for reducing or completely offsetting relative motion between the implant components, thereby further reducing wear of a sealing part of the elastomer seal due to the relative motion between the parts. According to the present invention, the seal is tightly attached to in vivo implant components, such that the wear debris cannot escape, and a friction force between the seal and the in vivo implant is smaller than a force for driving the components to generate relative motion, such that the relative motion between the components may not be blocked, thereby solving the problem of wear debris escaping.

Techniques for implantable orthopedic pain management devices are disclosed, including incising an opening in a synovial capsule substantially surrounding a joint, using a first tool to form an enlarged opening in the synovial capsule, determining whether to modify the joint, the joint being modified using a second tool if a bone structure coupled to one or more bones is found within the joint and the bone structure is configured to limit articulation of the one or more bones when an implantable device is inserted into the synovial capsule and the joint, and inserting the implantable device into the synovial capsule through the enlarged opening, the implantable device being inserted into the joint using a third tool.

The present invention discloses a zonal trabecular uni-compartmental tibial plateau containing zirconium-niobium alloy on oxidation layer and preparation method, including following steps: using zirconium niobium alloy powder as raw material, conducting a 3D printing for one-piece molding to obtain an intermediate product of the uni-compartmental tibial plateau, performing hot isostatic pressing and cryogenic oxidation to obtain the uni-compartmental tibial plateau; the lower surface of the semi-tibial plateau support and the surface of the keel plate are both provided with a bone trabeculae; the zonal trabecular uni-compartmental tibial plateau adopts the structure of arranging step distributed bone trabeculaes which can reduce the fretting wear of the interface between the prosthesis and the bone, and reduce the stress shielding effect of the prosthesis on the bone tissue, homogenize the stress of the tibial plateau bone tissue, and improve the initial stability and long-term stability of the uni-compartmental tibial plateau.