A non-bioabsorbable device designed to be implanted into the first carpometacarpal (CMC) joint (i.e., between the trapezium and the first metacarpal bone) to treat pain, instability, and/or motion disabilities of the thumb caused by arthritis. It is typically
| Company | Devices | Share |
|---|---|---|
| Biopro, Inc. | 50 | 94% |
| Tornier | 3 | 6% |
Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| KYI | Prosthesis, Wrist, Carpal Trapezium | 50 |
| KYI | PROSTHESIS, WRIST, CARPAL TRAPEZIUM | 3 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
53 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Carpometacarpal interpositional spacer, non-bioabsorbable", from 2 companies. The largest labeler is Biopro, Inc. with 94% of records.
KYI (Prosthesis, Wrist, Carpal Trapezium), KYI (PROSTHESIS, WRIST, CARPAL TRAPEZIUM)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.