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Data / Medical devices / Container, Specimen, Non-Sterile / United Kingdom

FDA-registered makers of Container, Specimen, Non-Sterile in the United Kingdom: 7 establishments

7 establishments in the United Kingdom are registered with the FDA to make Container, Specimen, Non-Sterile (product code NNI). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Container, Specimen, Non-Sterile
Product code
NNI
Country
United Kingdom

Makers of Container, Specimen, Non-Sterile in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cybertools Ltd.Buntingford Hertfordshire, United KingdomContract manufacturer, Manufacturer0000api.fda.gov
Medical Transportation Devices LimitedAylesford Kent, United KingdomManufacturer0000api.fda.gov
Purple Surgical International LimitedHerts England, United KingdomManufacturer0000api.fda.gov
Purple Surgical Manufacturing LimitedTaunton Somerset, United KingdomManufacturer0000api.fda.gov
Real Digital International LimitedSurrey England, United KingdomManufacturer0000api.fda.gov
Vacsax LimitedPlymouth Devon, United KingdomManufacturer0000api.fda.gov
Vernacare Ltd.Bolton Lancashire, United KingdomManufacturer0000api.fda.gov

Updated November 3, 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.