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Data / Medical devices / Drape, Surgical, Antimicrobial / Mexico

FDA-registered makers of Drape, Surgical, Antimicrobial in Mexico: 13 establishments

13 establishments in Mexico are registered with the FDA to make Drape, Surgical, Antimicrobial (product code KKX). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Drape, Surgical, Antimicrobial
Product code
KKX
Country
Mexico

Makers of Drape, Surgical, Antimicrobial in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Arrow Internacional de Chihuahua S.A. de C.V.Chihuahua, MexicoExporter to the US, Manufacturer, Repackager or relabeler15November 9, 2010000api.fda.gov
La Ada de AcunaCIUDAD DE ACUNA Coahuila, MexicoManufacturer4November 9, 2010000api.fda.gov
La Ada De Acuna, S. de. R. L. de C. V.COL.EDUCATIVA,NOGALES Sonora, MexicoManufacturer3November 9, 2010000api.fda.gov
Industrias Apson S.A de C.VAGUA PRIETA Sonora, MexicoContract manufacturer, Manufacturer1October 20, 1997000api.fda.gov
SOLVENTUM US LLC (Apodaca)Apodaca Nuevo Leon, MexicoManufacturer1September 17, 1981000api.fda.gov
3M Edumex, S.A De C.VCD. JUAREZ Chihuahua, MexicoContract manufacturer0000api.fda.gov
Ammar Apparel Ii S. De R.L De C.V.CALKINI Campeche, MexicoContract manufacturer0000api.fda.gov
HARMAC MEDICAL PRODUCTS, INC./H3 de Tijuana, S. de RL de C.V.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Maquiladora De Coahuila S De RL De CVCUIDAD ACUNA Coahuila, MexicoContract manufacturer0000api.fda.gov
NPA de México S. de R.L. de C.V.TIJUANA Baja California, MexicoContract manufacturer0000api.fda.gov
Suministros Y Desechables Skkyd S.A. De C.V.Naucalpan Estado de Mexico, MexicoExporter to the US, Manufacturer, Specification developer0000api.fda.gov
Tecma Operaciones S. De R.L. De C.V.Juarez Chihuahua, MexicoContract manufacturer0000api.fda.gov
Wear Tex S. De R.L. De C.V.Torreon Coahuila, MexicoContract manufacturer0000api.fda.gov

Updated November 3, 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.