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Data / Medical devices / Oximeter / Mexico

FDA-registered makers of Oximeter in Mexico: 7 establishments

7 establishments in Mexico are registered with the FDA to make Oximeter (product code DQA). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Oximeter
Product code
DQA
Country
Mexico

Makers of Oximeter in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Industrial Vallera de Mexicali, S. A. de C. V.Mexicali Mexico, MexicoManufacturer31December 15, 2023000api.fda.gov
CovidienTIJUANA, B.C. Mexico, MexicoManufacturer6May 6, 2022000api.fda.gov
Industrial Vallera de Mexicali, S.A. de C.V. (Terra)Mexicali Baja California, MexicoManufacturer6December 15, 2023000api.fda.gov
GE Medical Systems Information Technologies - Critikon de Mexico S. de R.L. de C.V.JUAREZ Chihuahua, MexicoManufacturer1March 12, 2010000api.fda.gov
Stryker Tijuana OperationsTijuana Baja California, MexicoReprocessor1March 8, 2022000api.fda.gov
NextPhase Medical Devices Mexico LLCTIJUANA Baja California, MexicoContract manufacturer0000api.fda.gov
Velcromex, S.A. De C.V.AGUA PRIETA Sonora, MexicoContract manufacturer0000api.fda.gov

Updated November 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.