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Data / Medical devices / Protector, Ostomy / United Kingdom

FDA-registered makers of Protector, Ostomy in the United Kingdom: 7 establishments

7 establishments in the United Kingdom are registered with the FDA to make Protector, Ostomy (product code EXE). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Protector, Ostomy
Product code
EXE
Country
United Kingdom

Makers of Protector, Ostomy in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Clinical Polymer Technologies LtdCoalville Leicestershire, United KingdomContract manufacturer0000api.fda.gov
Convatec LimitedDeeside Flintshire, United KingdomManufacturer0000api.fda.gov
ConvaTec Limited, GDC BuildingDeeside Flintshire, United KingdomSpecification developer0000api.fda.gov
Gbuk Group LimitedSelby North Yorkshire, United KingdomSpecification developer0000api.fda.gov
Medicina LtdBlackrod Bolton, United KingdomComplaint file establishment, Specification developer0000api.fda.gov
Pharmapac (UK) LtdBidston Wirral, United KingdomContract manufacturer0000api.fda.gov
T.G. Eakin, Ltd.COMBER, COUNTY DOWN Ards and North Down, United KingdomManufacturer0010api.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.