Met One Technologies, LLC
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories4
Latest Approval2026-02-12
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K251732 | Wrist Fracture System | HRS | 2026-02-12 | View |
| 510(k) | K250866 | Sovereign Posterior Cervical System | NKG | 2025-05-20 | View |
| 510(k) | K230851 | Kodiak Lumbar Spacer System | MAX | 2023-05-26 | View |
| 510(k) | K222806 | Kodiak C Spinal Implant System | ODP | 2022-12-22 | View |
No matching devices.