Cresilon, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2025-12-12
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253609 | TRAUMAGEL® 2.0 Hemostatic Gel | QSY | 2025-12-12 | View |
| 510(k) | K240713 | TRAUMAGEL® | QSY | 2024-08-14 | View |
| 510(k) | K213652 | Cresilon Hemostatic Gel, CHG, Cresilon Hemostatic Gel (CHG) | QSY | 2023-06-28 | View |
No matching devices.