Biomet, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Taperloc® Complete Hip Stem, Biomet Kirschner Wires (K-Wires), StageOne™ Select Hip Cement Spacer Molds
441
Total
419
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biomet, Inc. Orthopedic ✕
387 devices
Cleared
May 19, 2026
Taperloc® Complete Hip Stem
Orthopedic
390d
Cleared
May 22, 2024
Biomet Kirschner Wires (K-Wires)
Orthopedic
40d
Cleared
Dec 28, 2022
StageOne™ Select Hip Cement Spacer Molds
Orthopedic
106d
Cleared
Sep 15, 2022
StageOne™ Shoulder Cement Spacer Molds
Orthopedic
72d
Cleared
Sep 02, 2022
StageOne Knee Cement Spacer Molds
Orthopedic
336d
Cleared
Feb 07, 2022
Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve
Orthopedic
187d
Cleared
Dec 10, 2021
Comprehensive Humeral Fracture Positioning Sleeves
Orthopedic
128d
Cleared
Feb 19, 2021
A.L.P.S. Clavicle Plating System
Orthopedic
25d
Cleared
Nov 10, 2020
WasherLoc and No-Profile Screw and Washer Systems, Biomet Cannulated Screw...
Orthopedic
355d
Cleared
Sep 25, 2020
Distal Centralizers
Orthopedic
280d
Cleared
Apr 15, 2020
Comprehensive® Reverse Shoulder
Orthopedic
132d
Cleared
Mar 05, 2020
ALLthread PEEK Suture Anchor
Orthopedic
90d
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