Depuy, Inc.
United StatesFDA applicant, unverified
- Devices
- 307
What Depuy, Inc. makes
The company manufactures orthopedic implants and fixation systems, including femoral prostheses (revision and primary), cobalt-chrome hip components, titanium cross-pin fixation devices, and cannulated screw systems for bone stabilization. It also produces bone cement mixing systems, intramedullary nails, hemiarthroplasty shoulder prostheses, fracture stems, and zirconia total hip ball head systems, as well as collarless lateralized femoral hip implants.
These devices are regulated under FDA classifications, including Class I, Class II, and Class III, with many cleared via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Search and filter all 307 devicesCement Chisels Ref K770205
Regimes: 510(k) Registry: 510(k)- Regimes: PMA Registry: PMA
Depuy 3 Bone Cement Ref P960001
Regimes: PMA Registry: PMAProsthesis, Hip, Hemi-Femoral, Metal Ref K914078
Regimes: PMA 510(k) Registry: PMACmw Orthopaedic Bone Cement Ref N18466
Regimes: PMA Registry: PMANew Jersey Lcs(R) Total Knee System Ref P910016
Regimes: PMA, withdrawn Registry: PMANew Jersey Lcs(R) Total Knee System Ref P830055
Regimes: PMA Registry: PMA
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