Biomet Orthopedics
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories4
Latest Approval2026-04-15
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K252404 | Comprehensive Reverse Shoulder - HA Glenosphere Baseplates | PHX | 2026-04-15 | View |
| 510(k) | K243761 | A.L.P.S. Small Fragment Plating System | HRS | 2025-02-19 | View |
| 510(k) | K223631 | Comprehensive Segmental Revision System(SRS) | KWT | 2023-07-12 | View |
| 510(k) | K200196 | Taperloc® Complete Hip Stems | LZO | 2020-12-08 | View |
No matching devices.