Home › Device types › KWB
Prosthesis, Hip, Hemi-, Acetabular, Cemented, Metal
FDA product code KWB · Class 3 · Orthopedic
37
Registered devices
6,779
Adverse events
0
Recalls
0
510(k) clearances
Devices with this code
TAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY INSTRUMENTATION — Biomet Uk LtdU.L.I.S.™ — SPINEVISIONTAPERLOC — Biomet Orthopedics, LLCTAPERLOC — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCIMPLANET SPINE SYSTEM — IMPLANETTAPERLOC — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTaperloc® Microplasty® — Biomet Orthopedics, LLCTaperloc® Microplasty® — Biomet Orthopedics, LLCTaperloc® Microplasty® — Biomet Orthopedics, LLCTaperloc® Microplasty® — Biomet Orthopedics, LLCTaperloc® Microplasty® — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTAPERLOC MICROPLASTY HIP SYSTEM — Biomet Orthopedics, LLCTaperloc® Microplasty® — Biomet Orthopedics, LLC
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.