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Data / Medical devices / Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented / Ireland

FDA-registered makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented in Ireland: 6 establishments

6 establishments in Ireland are registered with the FDA to make Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented (product code LWJ). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
Product code
LWJ
Country
Ireland

Makers of Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Depuy (ireland)CO. CORK Munster, IrelandManufacturer, Repackager or relabeler1April 1, 1992000api.fda.gov
Depuy Ireland UCCo. Cork Munster, IrelandManufacturer, Specification developer1April 1, 1992000api.fda.gov
Stryker Ireland OsteonicsCounty Cork, IrelandManufacturer, Specification developer1November 16, 1999000api.fda.gov
Aps Materials Inc. IrelandWaterford Waterford(County), IrelandContract manufacturer0000api.fda.gov
Howmedica International S. De R.L.LIMERICK Munster, IrelandManufacturer0000api.fda.gov
Stryker AnngroveCork Munster, IrelandContract manufacturer0000api.fda.gov

Updated November 2, 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.