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Data / Medical devices / Humidifier, Non-Direct Patient Interface (Home-Use) / Mexico

FDA-registered makers of Humidifier, Non-Direct Patient Interface (Home-Use) in Mexico: 6 establishments

6 establishments in Mexico are registered with the FDA to make Humidifier, Non-Direct Patient Interface (Home-Use) (product code KFZ). 0 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
Humidifier, Non-Direct Patient Interface (Home-Use)
Product code
KFZ
Country
Mexico

Makers of Humidifier, Non-Direct Patient Interface (Home-Use) in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Industrias Apson S.A de C.VAGUA PRIETA Sonora, MexicoContract manufacturer0000api.fda.gov
Key Tronic Juarez, S.A de C.V.Juarez Chihuahua, MexicoContract manufacturer0000api.fda.gov
Productos Urologos De Mexico S.A. De C.V.MEXICALI Baja California, MexicoContract manufacturer0000api.fda.gov
WESTMED de Mexico, S.A de C.V.Tecate Baja California, MexicoManufacturer0000api.fda.gov
Westmed Javid de Mexico, S.A. de C.V.NOGALES Sonora, MexicoManufacturer0000api.fda.gov
Westmed de Mexico, S.A de C.VNOGALES 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.