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Biomet Manufacturing Corp

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
128
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K230540Patient Specific Planning Solution™ 3D Bone ModelsJuly 25, 2023
K214001Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder SystemMarch 15, 2023
K211729Comprehensive® Convertible Glenoid - Vivacit-E LinerNovember 4, 2021
K202232Comprehensive Vault Reconstruction SystemFebruary 19, 2021
K193038Comprehensive Shoulder SystemOctober 28, 2020
K182516Comprehensive Nano Stemless ShoulderApril 22, 2019
K181611Comprehensive Reverse Shoulder SystemSeptember 24, 2018
K173411Comprehensive Segmental Revision System (SRS)February 8, 2018
K172502Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate, Comprehensive Mini BasJanuary 3, 2018
K163651ExpressBraid Graft ManipulationFebruary 17, 2017
K152754COMPREHENSIVE VAULT RECONSTRUCTION SYSTEM (VRS)May 16, 2016
K153558Ventix Suture AnchorApril 21, 2016
K152262Ventix Knotless AnchorsMarch 8, 2016
K152868ExpressBraid Graft ManipulationFebruary 8, 2016
K153398Comprehensive SRS/Nexel ElbowFebruary 3, 2016
K151615TiTHON Staple with OsseoTi TechnologyOctober 2, 2015
K150768JuggerKnot Soft AnchorsSeptember 4, 2015
K142814Biomet Orthopaedic Salvage System (OSSTM) - Proximal Femoral & Hybrid TibialJune 25, 2015
K150424JuggerStitch Meniscal Repair DeviceMay 15, 2015
K143697Biomet Proximal Humerus Plating SystemMarch 30, 2015