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Data / Medical devices / Shoulder Prosthesis, Reverse Configuration / Ireland

FDA-registered makers of Shoulder Prosthesis, Reverse Configuration in Ireland: 7 establishments

7 establishments in Ireland are registered with the FDA to make Shoulder Prosthesis, Reverse Configuration (product code PHX). 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
Shoulder Prosthesis, Reverse Configuration
Product code
PHX
Country
Ireland

Makers of Shoulder Prosthesis, Reverse Configuration in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Depuy Ireland UCCo. Cork Munster, IrelandManufacturer, Specification developer16March 11, 2026000api.fda.gov
Depuy (ireland)CO. CORK Munster, IrelandManufacturer, Specification developer11October 4, 2019000api.fda.gov
Stryker MacroomCo Cork Munster, IrelandContract manufacturer, Manufacturer5November 15, 2016000api.fda.gov
Aps Materials Inc. IrelandWaterford Waterford(County), IrelandContract manufacturer0000api.fda.gov
Croom Precision MedicalCroom Limerick(County), IrelandContract manufacturer0000api.fda.gov
Stryker Ireland OsteonicsCounty Cork, IrelandContract manufacturer0000api.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.