Biomet, Inc.
FDA 510(k) & PMA Approved Devices — 36 products
Total Devices36
Categories19
Latest FDA decision2026-07-01
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253434 | OSSTM Orthopedic Salvage System | JDI | 2026-07-01 | View |
| 510(k) | K251270 | Taperloc® Complete Hip Stem | LPH | 2026-05-19 | View |
| 510(k) | K241014 | Biomet Kirschner Wires (K-Wires) | HTY | 2024-05-22 | View |
| 510(k) | K222760 | StageOne™ Select Hip Cement Spacer Molds | MBB | 2022-12-28 | View |
| 510(k) | K221968 | StageOne™ Shoulder Cement Spacer Molds | MBB | 2022-09-15 | View |
| 510(k) | K213287 | StageOne Knee Cement Spacer Molds | MBB | 2022-09-02 | View |
| 510(k) | K212431 | Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve | JDG | 2022-02-07 | View |
| 510(k) | K212435 | Comprehensive Humeral Fracture Positioning Sleeves | KWS | 2021-12-10 | View |
| 510(k) | K210192 | A.L.P.S. Clavicle Plating System | HRS | 2021-02-19 | View |
| 510(k) | K193214 | WasherLoc and No-Profile Screw and Washer Systems, Biomet Cannulated Screw System, Biomet Headless Compression and Twist-Off Screws | MBI | 2020-11-10 | View |
| 510(k) | K193546 | Distal Centralizers | JDG | 2020-09-25 | View |
| 510(k) | K193373 | Comprehensive® Reverse Shoulder | PHX | 2020-04-15 | View |
| 510(k) | K193402 | ALLthread PEEK Suture Anchor | MBI | 2020-03-05 | View |
| 510(k) | K193451 | Titanium Interference Screws | HWC | 2020-02-24 | View |
| 510(k) | K193533 | WIN Flexible Nail System | JDS | 2020-02-20 | View |
| 510(k) | K192942 | ALLthread Titanium Suture Anchor | MBI | 2020-01-16 | View |
| 510(k) | K193092 | TunneLoc Tibial Fixation Device | MBI | 2020-01-02 | View |
| 510(k) | K191459 | JuggerStitch Meniscal Repair Device | MBI | 2019-09-13 | View |
| 510(k) | K190035 | Biomet Headless Compression and Twist-Off Screws | HWC | 2019-02-07 | View |
| 510(k) | K183553 | Compress and Mini Compress Anti-Rotation Spindles | MBF | 2019-01-22 | View |
No matching devices.
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