Biomet Manufacturing Corp - FDA 510(k) Cleared Devices
93
Total
93
Cleared
0
Denied
Biomet Manufacturing Corp has 93 FDA 510(k) cleared orthopedic devices. Based in Warsaw, US.
Last cleared in 2023. Active since 2004.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Biomet Manufacturing Corp
93 devices
Cleared
Jul 25, 2023
Patient Specific Planning Solution™ 3D Bone Models
Radiology
148d
Cleared
Mar 15, 2023
Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder System
Orthopedic
449d
Cleared
Nov 04, 2021
Comprehensive® Convertible Glenoid - Vivacit-E Liner
Orthopedic
153d
Cleared
Feb 19, 2021
Comprehensive Vault Reconstruction System
Orthopedic
196d
Cleared
Oct 28, 2020
Comprehensive Shoulder System
Orthopedic
363d
Cleared
Apr 22, 2019
Comprehensive Nano Stemless Shoulder
Orthopedic
221d
Cleared
Sep 24, 2018
Comprehensive Reverse Shoulder System
Orthopedic
97d
Cleared
Feb 08, 2018
Comprehensive Segmental Revision System (SRS)
Orthopedic
99d
Cleared
Jan 03, 2018
Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate,...
Orthopedic
138d
Cleared
Feb 17, 2017
ExpressBraid Graft Manipulation
General & Plastic Surgery
56d
Cleared
May 16, 2016
COMPREHENSIVE VAULT RECONSTRUCTION SYSTEM (VRS)
Orthopedic
235d
Cleared
Apr 21, 2016
Ventix Suture Anchor
Orthopedic
129d
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