Biomet Orthopedics - FDA 510(k) Cleared Devices
Recent clearances: Comprehensive Reverse Shoulder - HA Glenosphere Baseplates, A.L.P.S. Small Fragment Plating System, Comprehensive Segmental Revision System(SRS)
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biomet Orthopedics Orthopedic ✕
4 devices
Cleared
Apr 15, 2026
Comprehensive Reverse Shoulder - HA Glenosphere Baseplates
Orthopedic
258d
Cleared
Feb 19, 2025
A.L.P.S. Small Fragment Plating System
Orthopedic
75d
Cleared
Jul 12, 2023
Comprehensive Segmental Revision System(SRS)
Orthopedic
219d
Cleared
Dec 08, 2020
Taperloc® Complete Hip Stems
Orthopedic
316d