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Data / Medical devices / Valve, Non-Rebreathing / Mexico

FDA-registered makers of Valve, Non-Rebreathing in Mexico: 6 establishments

6 establishments in Mexico are registered with the FDA to make Valve, Non-Rebreathing (product code CBP). 3 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
Valve, Non-Rebreathing
Product code
CBP
Country
Mexico

Makers of Valve, Non-Rebreathing in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Productos Urologos De Mexico S.A. De C.V.MEXICALI Baja California, MexicoManufacturer1March 12, 1979000api.fda.gov
WESTMED de Mexico, S.A de C.V.Tecate Baja California, MexicoContract manufacturer, Manufacturer1February 3, 1992000api.fda.gov
Westmed Javid de Mexico, S.A. de C.V.NOGALES Sonora, MexicoContract manufacturer, Manufacturer1February 3, 1992000api.fda.gov
ICU Medical Healthcare Manufacturing S.A. de C.V.APODACA Nuevo Leon, MexicoManufacturer0000api.fda.gov
S & Mohr America, S.A. DE C.V.ESTADO DE MEXICO Ciudad de Mexico, MexicoContract manufacturer0000api.fda.gov
Teleflex Medical de Mexico, S. de R.L. de C.V.NUEVO LAREDO Tamaulipas, 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.