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Data / Medical devices / Catheter, Electrode Recording, Or Probe, Electrode Recording / Mexico

FDA-registered makers of Catheter, Electrode Recording, Or Probe, Electrode Recording in Mexico: 7 establishments

7 establishments in Mexico are registered with the FDA to make Catheter, Electrode Recording, Or Probe, Electrode Recording (product code DRF). 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
Catheter, Electrode Recording, Or Probe, Electrode Recording
Product code
DRF
Country
Mexico

Makers of Catheter, Electrode Recording, Or Probe, Electrode Recording in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cordis de Mexico, SA de CVJUAREZ Chihuahua, MexicoManufacturer26January 26, 2022100api.fda.gov
Arrow Internacional de Chihuahua S.A. de C.V.Chihuahua, MexicoExporter to the US, Manufacturer1August 8, 1995000api.fda.gov
Medtronic Mexico S. de R.L. de CVTijuana Baja California, MexicoManufacturer1March 18, 2011000api.fda.gov
Bard Reynosa S.A. De C.V.REYNOSA Tamaulipas, MexicoContract manufacturer0000api.fda.gov
Foxconn Baja California S.A De C.V.tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Molex S.A. De C.V.Nogales Sonora, MexicoContract manufacturer0000api.fda.gov
Venusa de Mexico S. de R.L de C.VCIUDAD JUAREZ Chihuahua, 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.