Medical Device Manufacturer · US , Washington , DC

Leibinger GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

Recent clearances: BONE-LOCK

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Leibinger GmbH Dental ✕

1 devices

1-1 of 1

Cleared Nov 14, 1997