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Data / Medical devices / Adjunctive Cardiovascular Status Indicator

Adjunctive Cardiovascular Status Indicator (PPW): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Adjunctive Cardiovascular Status Indicator (product code PPW, Class 2, 21 CFR 870.2200). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 8 510(k) clearances under this code, the latest on April 3, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
PPW
Device class
2
Regulation
870.2200
Medical specialty
Cardiovascular

Makers by country

CountryMakers
United States2
Canada1

Makers of Adjunctive Cardiovascular Status Indicator

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
Etiometry Inc.Dedham, MA, United StatesManufacturer3February 12, 2025000api.fda.gov
Prolaio Inc.Chicago, IL, United StatesManufacturer1December 16, 2025000api.fda.gov
Opsens Inc.Quebec City, CanadaManufacturer0000api.fda.gov

Updated April 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.