Skip to the page

Data / Medical devices / Spirometer, Therapeutic (Incentive) / Mexico

FDA-registered makers of Spirometer, Therapeutic (Incentive) in Mexico: 6 establishments

6 establishments in Mexico are registered with the FDA to make Spirometer, Therapeutic (Incentive) (product code BWF). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 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.

Device
Spirometer, Therapeutic (Incentive)
Product code
BWF
Country
Mexico

Makers of Spirometer, Therapeutic (Incentive) in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Rci Hudson De Mexico S. De RL. De CV.Nuevo Laredo Tamaulipas, MexicoManufacturer4October 25, 2022000api.fda.gov
Tecnologias Medicas Innovadoras S De RLH. MATAMOROS Tamaulipas, MexicoManufacturer3May 27, 2016000api.fda.gov
ICU Medical Healthcare Manufacturing S.A. de C.V.Tijuana, B.C. C.P. Baja California, MexicoManufacturer1October 8, 1976000api.fda.gov
Productos Urologos De Mexico S.A. De C.V.MEXICALI Baja California, MexicoManufacturer1September 26, 1979000api.fda.gov
Manufactura Integrada Del PacificoTijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Teleflex Medical de Tecate, S. de R.L de C.V.TECATE Baja California, MexicoManufacturer0000api.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.