Data / Medical devices / Oximeter

Oximeter (DQA): 245 FDA-registered makers in 30 countries

245 establishments in 30 countries are registered with the FDA to make Oximeter (product code DQA, Class 2, 21 CFR 870.2700). 117 of them have a 510(k) clearance or PMA approval on file and 12 have a recall event. The FDA has issued 727 510(k) clearances under this code, the latest on October 2, 2026, and lists 46 recall events (0 Class I). FDA data exported November 3, 2026.

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Product code

DQA

Device class

2

Regulation

870.2700

Medical specialty

Cardiovascular

Makers by country

Makers of Oximeter

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.

Updated October 2, 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.