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Data / Medical devices / Aortic Annuloplasty Ring

Aortic Annuloplasty Ring (PST): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Aortic Annuloplasty Ring (product code PST, Class 2, 21 CFR 870.3800). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on August 10, 2017, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
PST
Device class
2
Regulation
870.3800
Medical specialty
Cardiovascular
Implant
Yes
Life sustaining or supporting
Yes

Makers by country

CountryMakers
United States2
Italy1

Makers of Aortic Annuloplasty Ring

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
Corcym Inc.Englewood, CO, United StatesManufacturer2August 10, 2017000api.fda.gov
Corcym S.r.l.SALUGGIA Vercelli, ItalyContract manufacturer0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, United StatesContract manufacturer0000api.fda.gov

Updated August 10, 2017. 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.