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Data / Medical devices / Wire, Guide, Catheter / Ireland

FDA-registered makers of Wire, Guide, Catheter in Ireland: 6 establishments

6 establishments in Ireland are registered with the FDA to make Wire, Guide, Catheter (product code DQX). 6 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
Wire, Guide, Catheter
Product code
DQX
Country
Ireland

Makers of Wire, Guide, Catheter in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Boston Scientific LimitedGALWAY Galway(County), IrelandManufacturer23September 26, 2018000api.fda.gov
Brivant, Ltd.GALWAY Galway(County), IrelandComplaint file establishment, Contract manufacturer, Manufacturer11March 19, 2026000api.fda.gov
Merit Medical Ireland, LtdGalway Galway(County), IrelandContract manufacturer, Repackager or relabeler4March 31, 1994000api.fda.gov
Lake Region Medical LimitedNEW ROSS Wexford, IrelandContract manufacturer, Manufacturer3December 17, 2014000api.fda.gov
Boston Scientific LimitedCORK Munster, IrelandManufacturer1November 9, 2017000api.fda.gov
Phenox LimitedGalway Galway(County), IrelandManufacturer1October 9, 2019000api.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.