BROACH
FDA product code HTQ · Class 1 · 121 devices · 3,979 reports · 0 devices named in recalls
- ATTUNE 2511-01-105Depuy (Ireland) · BROACH2 reports
- ATTUNE 2511-01-106Depuy (Ireland) · BROACH2 reports
- AETOS Shoulder System COM-0990-808-03Smith & Nephew, Inc. · BROACH1 report
- SILICONE PIP 17-0863Stryker GmbH · BROACH1 report
- SILICONE PIP 17-0869Stryker GmbH · BROACH1 report
- LMH 62001001Wright Medical Technology, Inc. · BROACH1 report
- Integra® Freedom Wrist Arthroplasty System 348169Ascension Orthopedics, Inc. · BROACH1 report
- TRI-LOCK 2012-03-080Depuy (Ireland) · BROACH1 report
- TRI-LOCK 2012-03-090Depuy (Ireland) · BROACH1 report
- TRI-LOCK 2012-03-110Depuy (Ireland) · BROACH1 report
- TRI-LOCK 2012-03-120Depuy (Ireland) · BROACH1 report
- GLOBAL ADVANTAGE 2128-60-010Depuy (Ireland) · BROACH1 report
- GLOBAL AP 2130-01-085Depuy Orthopaedics, Inc. · BROACH1 report
- GLOBAL 2235-02-000Depuy Orthopaedics, Inc. · BROACH1 report
- NA 2299-90-016Depuy Orthopaedics, Inc. · BROACH1 report
- NA 96-1685Depuy (Ireland) · BROACH1 report
- CORAIL L20420Depuy (Ireland) · BROACH1 report
- ATTUNE 2511-11-104Depuy (Ireland) · BROACH1 report
- ATTUNE 2511-11-105Depuy (Ireland) · BROACH1 report
- ATTUNE 2511-01-107Depuy (Ireland) · BROACH1 report
- PROFEMUR® PRGLSTBRMicroport Orthopedics Inc. · BROACH1 report