Medical Device Manufacturer · US , Parsippany , NJ

Biomet Trauma (Aka Ebi, Lp) - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2010

Total

Cleared

Denied

Biomet Trauma (Aka Ebi, Lp) has 3 FDA 510(k) cleared medical devices. Based in Parsippany, US.

Historical record: 3 cleared submissions from 2010 to 2010. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Biomet Trauma (Aka Ebi, Lp) Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biomet Trauma (Aka Ebi, Lp)

3 devices

1-3 of 3