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Data / Medical devices / Prosthesis, Hip, Hemi-, Femoral, Metal / Ireland

FDA-registered makers of Prosthesis, Hip, Hemi-, Femoral, Metal in Ireland: 7 establishments

7 establishments in Ireland are registered with the FDA to make Prosthesis, Hip, Hemi-, Femoral, Metal (product code KWL). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Prosthesis, Hip, Hemi-, Femoral, Metal
Product code
KWL
Country
Ireland

Makers of Prosthesis, Hip, Hemi-, Femoral, Metal in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Stryker Ireland OsteonicsCounty Cork, IrelandManufacturer, Specification developer3September 1, 1999000api.fda.gov
Depuy (ireland)CO. CORK Munster, IrelandManufacturer, Repackager or relabeler, Specification developer1February 12, 1993000api.fda.gov
Depuy Ireland UCCo. Cork Munster, IrelandManufacturer, Specification developer1May 15, 2026000api.fda.gov
Aps Materials Inc. IrelandWaterford Waterford(County), IrelandContract manufacturer0000api.fda.gov
Howmedica International S. De R.L.LIMERICK Munster, IrelandManufacturer0000api.fda.gov
Signature Orthopaedics Europe LtdAthlone Westmeath, 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.