Armis Biopharma, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-05-25
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220759 | Armis VeriCyn Wound Wash | FQH | 2023-05-25 | View |
| 510(k) | K202777 | VeriFixx™ Small Bone Implant | HTY | 2020-11-17 | View |
No matching devices.