Imtec Corp. - FDA 510(k) Cleared Devices
Recent clearances: MDI MII ONE-PIECE IMPLANT, 2.9MM, ILUMA VISION, ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114
28
Total
28
Cleared
0
Denied
FDA 510(k) Regulatory Record - Imtec Corp. Obstetrics & Gynecology ✕
2 devices