Keri Medical SA
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-06-24
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P240020 | Prosthesis, finger, semi-constrained, metal/polymer | SFA | 2026-06-24 | View |
| 510(k) | K211385 | KeriFlex® MCP and PIP Finger Joint Prostheses | KYJ | 2022-07-27 | View |
No matching devices.