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Data / Medical devices / Port & Catheter, Implanted, Subcutaneous, Intravascular / Mexico

FDA-registered makers of Port & Catheter, Implanted, Subcutaneous, Intravascular in Mexico: 6 establishments

6 establishments in Mexico are registered with the FDA to make Port & Catheter, Implanted, Subcutaneous, Intravascular (product code LJT). 2 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
Port & Catheter, Implanted, Subcutaneous, Intravascular
Product code
LJT
Country
Mexico

Makers of Port & Catheter, Implanted, Subcutaneous, Intravascular 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, MexicoManufacturer15March 1, 2010000api.fda.gov
Arrow Internacional de Chihuahua S.A. de C.V.Chihuahua, MexicoExporter to the US, Manufacturer, Repackager or relabeler1October 27, 2000000api.fda.gov
Bard Reynosa S.A. De C.V.REYNOSA Tamaulipas, MexicoContract manufacturer0000api.fda.gov
Grupo American Industries, S.A. De C.VCiudad Juarez Chihuahua, MexicoContract manufacturer0000api.fda.gov
Integra Biotechnical, SA de CVTijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Martech Medical Products S. De RL. De CV.MEXICALI 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.