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Data / Medical devices / Pump, Infusion / Mexico

FDA-registered makers of Pump, Infusion in Mexico: 12 establishments

12 establishments in Mexico are registered with the FDA to make Pump, Infusion (product code FRN). 6 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
Pump, Infusion
Product code
FRN
Country
Mexico

Makers of Pump, Infusion in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Avent S. de R.L. de C.V.TIJUANA Baja California, MexicoManufacturer, Repackager or relabeler3December 8, 2005000api.fda.gov
ICU Medical Healthcare Manufacturing S.A. de C.V.Tijuana, B.C. C.P. Baja California, MexicoManufacturer2November 17, 2005000api.fda.gov
S & Mohr America, S.A. DE C.V.ESTADO DE MEXICO Ciudad de Mexico, MexicoManufacturer2December 11, 2014000api.fda.gov
Cardinal Health (Kenmex Medical Specialties)TIJUANA Baja California, MexicoManufacturer1August 13, 1980000api.fda.gov
Haemonetics Mexico Manufacturing S. de R.L. de C.V.TIJUANA, B.C. Mexico, MexicoManufacturer1December 9, 1985000api.fda.gov
ICU MEDICAL DE MEXICO, S. de R.L. de C.V.ENSENADA, Baja California, MexicoManufacturer, Repackager or relabeler1January 16, 2015000api.fda.gov
AvailMed S.A.De C.V.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. S.A. de C.V.NOGALES Sonora, MexicoContract manufacturer0000api.fda.gov
Integra Biotechnical, SA de CVTijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Manufacturas Y Servicios Internacionales, S. De R.L.Cd Juarez Chihuahua, MexicoContract manufacturer0000api.fda.gov
RM Healthcare Products SA de CVJUAREZ Chihuahua, MexicoContract manufacturer0000api.fda.gov
Sistemas Medicos Alaris S.A de C.V.Tijuana Baja California, 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.