Biomet Trauma (Aka Ebi, Lp) is one of 20554 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomet Trauma (Aka Ebi, Lp) - FDA 510(k) Cleared Devices
Recent clearances: BIOMET FORERUNNER LOCKING PLATE SYSTEM, SMPLE PLATE AND SCREWS, OPTILOCK VL (VARIABLE ANGLE LOCKING) DISTAL RADIUS PLATING SYSTEM
3
Total
3
Cleared
0
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