Cresilon, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TRAUMAGEL® 2.0 Hemostatic Gel, TRAUMAGEL®, Cresilon Hemostatic Gel, CHG, Cresilon Hemostatic Gel (CHG)
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cresilon, Inc. General & Plastic Surgery ✕
3 devices