Data / Medical devices / Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented (KWY): 160 FDA-registered makers in 16 countries

160 establishments in 16 countries are registered with the FDA to make Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented (product code KWY, Class 2, 21 CFR 888.3390). 43 of them have a 510(k) clearance or PMA approval on file and 9 have a recall event. The FDA has issued 99 510(k) clearances under this code, the latest on April 13, 2026, and lists 23 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

KWY

Device class

2

Regulation

888.3390

Medical specialty

Orthopedic

Implant

Yes

Makers by country

Makers of Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated April 13, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.