Dio Medical Corporation
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories4
Latest Approval2022-10-25
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K222415 | Rexious Spinal Fixation System | NKB | 2022-10-25 | View |
| 510(k) | K222572 | FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM & BALTEUM-ONE Lumbar Plate System | KWQ | 2022-10-18 | View |
| 510(k) | K222448 | UNITY Sacroiliac Joint Fixation System | OUR | 2022-10-13 | View |
| 510(k) | K222515 | FaSet Fixation System | MRW | 2022-10-05 | View |
No matching devices.