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Data / Medical devices / Cannula, A-V Shunt

Cannula, A-V Shunt (FIQ): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Cannula, A-V Shunt (product code FIQ, Class 2, 21 CFR 876.5540). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 23 510(k) clearances under this code, the latest on May 15, 1989, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
FIQ
Device class
2
Regulation
876.5540
Medical specialty
Gastroenterology, Urology
Implant
Yes

Makers by country

CountryMakers
United States2
France1

Makers of Cannula, A-V Shunt

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
Covidien LLCMansfield, MA, United StatesSpecification developer2January 18, 1985000api.fda.gov
Mozarc Medical Us LLCMansfield, MA, United StatesSpecification developer2January 18, 1985000api.fda.gov
Vygon S AECOUEN 95440 Val-d'Oise, FranceManufacturer1July 7, 1983000api.fda.gov

Updated May 15, 1989. 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.