Data / Medical devices / Humidifier, Respiratory Gas, (Direct Patient Interface) / Mexico

FDA-registered makers of Humidifier, Respiratory Gas, (Direct Patient Interface) in Mexico: 17 establishments

Name: FDA-registered makers of Humidifier, Respiratory Gas, (Direct Patient Interface) in Mexico
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

17 establishments in Mexico are registered with the FDA to make Humidifier, Respiratory Gas, (Direct Patient Interface) (product code BTT). 9 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers of this device in Mexico Watch these makers

Device: Humidifier, Respiratory Gas, (Direct Patient Interface)
Product code: BTT
Country: Mexico

Makers of Humidifier, Respiratory Gas, (Direct Patient Interface) in Mexico

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Rci Hudson De Mexico S. De RL. De CV.	Nuevo Laredo Tamaulipas, Mexico	Manufacturer	15	July 2, 2025	api.fda.gov
Teleflex Medical de Tecate, S. de R.L de C.V.	TECATE Baja California, Mexico	Manufacturer	4	March 6, 2014	api.fda.gov
Baja Fur S.A. de C.V.	Tijuana Baja California, Mexico	Manufacturer, Repackager or relabeler	3	April 13, 2026	api.fda.gov
Productos Urologos De Mexico S.A. De C.V.	MEXICALI Baja California, Mexico	Contract manufacturer, Manufacturer	2	June 4, 1980	api.fda.gov
Salter Labs de Mexico de S.A. de C.V.	Chihuahua Mexico, Mexico	Contract manufacturer, Manufacturer	2	September 21, 2017	api.fda.gov
Covidien	TIJUANA, B.C. Mexico, Mexico	Manufacturer	1	November 19, 1976	api.fda.gov
ICU Medical Healthcare Manufacturing S.A. de C.V.	APODACA Nuevo Leon, Mexico	Manufacturer	1	September 18, 2000	api.fda.gov
WESTMED de Mexico, S.A de C.V.	Tecate Baja California, Mexico	Manufacturer	1	April 3, 1987	api.fda.gov
Westmed Javid de Mexico, S.A. de C.V.	NOGALES Sonora, Mexico	Contract manufacturer, Manufacturer	1	April 3, 1987	api.fda.gov
Fisher & Paykel Healthcare S.a.de C.V.	Tijuana, Baja California, Mexico	Contract manufacturer	0		api.fda.gov
Fisher & Paykel Healthcare S.A.de C.V.	Tijuana Baja California, Mexico	Contract manufacturer	0		api.fda.gov
Laboratorios PISA S.A. de C.V.	GUADALAJARA Jalisco, Mexico	Contract manufacturer, Contract sterilizer	0		api.fda.gov
Laboratorios PiSA, S. A. de C.V.	Tlajomulco de Zuniga Jalisco, Mexico	Contract manufacturer, Contract sterilizer	0		api.fda.gov
SEI Medical S.A. de C.V.	Juarez Chihuahua, Mexico	Contract manufacturer	0		api.fda.gov
TE Sensores S. de R.L. de C.V	Hermosillo Mexico, Mexico	Contract manufacturer	0		api.fda.gov
Teleflex Medical de Mexico, S. de R.L. de C.V.	NUEVO LAREDO Tamaulipas, Mexico	Contract manufacturer	0		api.fda.gov
Westmed de Mexico, S.A de C.V	NOGALES Sonora, Mexico	Contract manufacturer	0		api.fda.gov

Updated November 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.