Biomet Orthopedics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 39
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K243761 | A.L.P.S. Small Fragment Plating System | February 19, 2025 |
| K223631 | Comprehensive Segmental Revision System(SRS) | July 12, 2023 |
| K200196 | Taperloc® Complete Hip Stems | December 8, 2020 |
| K131393 | MAK OSS FEMORAL KNEE COMPONENTS | October 24, 2013 |
| K112905 | COMPRESS(R) SEGMENTAL HUMERAL REPLACEMENT SYSTEM | May 24, 2012 |
| K080528 | E-POLY TIBIAL BEARINGS | June 17, 2008 |
| K072879 | INNERVUE DIAGNOSTIC SCOPE SYSTEM | January 14, 2008 |
| K070955 | ACID ETCHED LAG SCREWS | October 12, 2007 |
| K033355 | LACTOSCREW SCREW ANCHOR | June 30, 2004 |
| K032286 | CALCIGEN PSI BONE GRAFT SUBSTITUTE | November 20, 2003 |
| K030048 | HA PMI FEMORAL HIP STEM | February 5, 2003 |
| K024086 | PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM | January 9, 2003 |
| K023063 | COMPREHENSIVE HUMERAL FRACTURE SYSTEM | December 13, 2002 |
| K023188 | PRESS-FIT HEAD RESURFACING DEVICE | December 11, 2002 |
| K023357 | ARCPM 1050 RESIN-HIPS | November 6, 2002 |
| K021661 | RINGLOC CONSTRAINED LINERS | October 25, 2002 |
| K023085 | RX 90 FEMORAL STEM AND RX 90 LATERALIZED FEMORAL STEM | October 17, 2002 |
| K022515 | BIOMET CALCANEAL PLATE | September 17, 2002 |
| K022463 | HA MODULAR REACH PROXIMAL POROUS AND HA MODULAR REACH COLLARED PROXIMAL POROUS FEMORAL STEMS | August 16, 2002 |
| K022586 | ANTERIOR STABILIZED TIBIAL BEARINGS | August 15, 2002 |