Osseofuse International, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2025-10-10
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K243078 | HexaPLUS S OneDrill Implant System | DZE | 2025-10-10 | View |
| 510(k) | K181157 | Conical Plus Implant System | DZE | 2019-05-24 | View |
No matching devices.