Medical Device Manufacturer · US , Cincinnati , OH

Sentron Medical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Recent clearances: SIS HERNIA REPAIR DEVICE

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sentron Medical, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared May 20, 1998

SIS HERNIA REPAIR DEVICE

General & Plastic Surgery · 168d