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Data / Medical devices / Protector, Skin Pressure / United Kingdom

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

7 establishments in the United Kingdom are registered with the FDA to make Protector, Skin Pressure (product code FMP). 0 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
Protector, Skin Pressure
Product code
FMP
Country
United Kingdom

Makers of Protector, Skin Pressure in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Care Surgical LimitedBurscough Lancashire, United KingdomContract manufacturer, Manufacturer0000api.fda.gov
First Water Ramsbury LtdMarlborough Wiltshire, United KingdomContract manufacturer0000api.fda.gov
Frontier Therapeutics LimitedTredegar Blaenau Gwent, United KingdomComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Medtrade Products Ltd.CHESHIRE Cheshire East, United KingdomManufacturer, Specification developer0000api.fda.gov
Neo G LimitedKnaresborough North Yorkshire, United KingdomManufacturer0000api.fda.gov
Prosys International LtdLondon London, City of, United KingdomExporter to the US, Specification developer0000api.fda.gov
Smith & Nephew Medical LtdHULL East Riding of Yorkshire, United KingdomManufacturer, Specification developer0000api.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.