Medical Device Manufacturer · US , San Diego , CA

Medartis AG - FDA 510(k) Cleared Devices

40 submissions · 40 cleared · Since 1999

40

Total

40

Cleared

0

Denied

FDA 510(k) cleared devices by Medartis AG Dental ✕

3 devices

1-3 of 3

Cleared Sep 11, 2007

MODUS TRILOCK 2.0/2.3/2.5

Cleared Nov 24, 1999

MODUS 2.5 MANDIBULAR RECONSTRUCTION SET

Cleared Nov 24, 1999

MODUS 2.5 MANDIBULAR TRAUMA SET