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Data / Medical devices / Dressing, Wound, Occlusive / United Kingdom

FDA-registered makers of Dressing, Wound, Occlusive in the United Kingdom: 13 establishments

13 establishments in the United Kingdom are registered with the FDA to make Dressing, Wound, Occlusive (product code NAD). 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
Dressing, Wound, Occlusive
Product code
NAD
Country
United Kingdom

Makers of Dressing, Wound, Occlusive in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Advanced Medical Solutions LtdWINSFORD Cheshire East, United KingdomManufacturer0000api.fda.gov
BDK Industrial Products LtdIpswich Suffolk, United KingdomContract manufacturer0000api.fda.gov
Brightwake LtdKirkby-in-Ashfield Nottinghamshire, United KingdomManufacturer0000api.fda.gov
Convatec LimitedDeeside Flintshire, United KingdomManufacturer0000api.fda.gov
ConvaTec Limited, GDC BuildingDeeside Flintshire, United KingdomSpecification developer0000api.fda.gov
Flexible Medical Packaging Ltd.LANCASTER Lancashire, United KingdomManufacturer0000api.fda.gov
Flexible Medical Packaging Ltd.MORECAMBE Lancashire, United KingdomContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Medtrade Products Ltd.CHESHIRE Cheshire East, United KingdomManufacturer, Specification developer0000api.fda.gov
Parafix Tapes & Conversions LimitedLancing West Sussex, United KingdomContract manufacturer0000api.fda.gov
Polarseal Tapes And Conversions LtdFarnham Surrey, United KingdomContract manufacturer0000api.fda.gov
Safeguard Medical Technologies LtdHereford Herefordshire, United KingdomSpecification developer0000api.fda.gov
Smith & Nephew Medical LtdHULL East Riding of Yorkshire, United KingdomForeign private label distributor, Manufacturer, Specification developer0000api.fda.gov
Systagenix Wound Management Manufacturing LimitedNorth Yorkshire, United KingdomContract manufacturer, Contract sterilizer0000api.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.