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Data / Medical devices / Catheters, Suction, Tracheobronchial / Mexico

FDA-registered makers of Catheters, Suction, Tracheobronchial in Mexico: 11 establishments

11 establishments in Mexico are registered with the FDA to make Catheters, Suction, Tracheobronchial (product code BSY). 1 has 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
Catheters, Suction, Tracheobronchial
Product code
BSY
Country
Mexico

Makers of Catheters, Suction, Tracheobronchial in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
ICU Medical Healthcare Manufacturing S.A. de C.V.Tijuana, B.C. C.P. Baja California, MexicoManufacturer1July 12, 1990000api.fda.gov
AVENT S. de R.L. de C.V.NOGALES Sonora, MexicoManufacturer0000api.fda.gov
Cardinal Health (Kenmex Medical Specialties)TIJUANA Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Industrias Plasticas Medicas, S.A. De C.V.Ayala Morelos, MexicoManufacturer0000api.fda.gov
Martech Medical Products S. De RL. De CV.MEXICALI Baja California, MexicoContract manufacturer0000api.fda.gov
Productos Para El Cuidado De La SaludNOGALES Sonora, MexicoContract manufacturer, Repackager or relabeler0000api.fda.gov
Productos Urologos De Mexico S.A. De C.V.MEXICALI Baja California, MexicoContract manufacturer0000api.fda.gov
Quiroproductos de Cuauhtemoc S. De R.L. de C.V.Cuauhtemoc Chihuahua, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Tri-State De Mexico, S. De R.L. De C.V.MEXICALI Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Westmed de Mexico, S.A de C.VNOGALES Sonora, MexicoContract manufacturer0000api.fda.gov
Westmed de Mexico, S.A de C.VMAGDALENA 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.