Medical Device Manufacturer · US , Washington , DC

Leibinger GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

Recent clearances: BONE-LOCK, LEIBINGER STEREOPLAN PLUS STEROTACTIC TREATMENT PLAN ING SOFTWARE PACKAGE, STP COMPLETE MODULE SET AND MASK FIXATION SYSTEM

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Nov 14, 1997