Ebi,Llc D/B/A Biomet Trauma is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ebi,Llc D/B/A Biomet Trauma - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ebi,Llc D/B/A Biomet Trauma has 1 FDA 510(k) cleared medical devices. Based in Parsippany, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ebi,Llc D/B/A Biomet Trauma Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ebi,Llc D/B/A Biomet Trauma
1 devices