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Data / Medical devices / Tube, Thorpe, Uncompensated

Tube, Thorpe, Uncompensated (BYM): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Tube, Thorpe, Uncompensated (product code BYM, Class 1, 21 CFR 868.2320). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on February 19, 1981, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
BYM
Device class
1
Regulation
868.2320
Medical specialty
Anesthesiology

Makers by country

CountryMakers
United Kingdom2
United States1

Makers of Tube, Thorpe, Uncompensated

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
BPR Medical LimitedMansfield Nottinghamshire, United KingdomManufacturer0000api.fda.gov
Hemostasis, LLCSaint Paul, MN, United StatesManufacturer0000api.fda.gov
Penlon Ltd.ABINGDON Oxfordshire, United KingdomManufacturer0000api.fda.gov

Updated February 19, 1981. 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.