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Data / Medical devices / Bedding, Disposable, Medical / Mexico

FDA-registered makers of Bedding, Disposable, Medical in Mexico: 13 establishments

13 establishments in Mexico are registered with the FDA to make Bedding, Disposable, Medical (product code KME). 0 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
Bedding, Disposable, Medical
Product code
KME
Country
Mexico

Makers of Bedding, Disposable, Medical in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3M Edumex, S.A De C.VCD. JUAREZ Chihuahua, MexicoContract manufacturer0000api.fda.gov
Articulos Mexicanos De Curacion S.A. De C.V.Mexico Ciudad de Mexico, MexicoManufacturer0000api.fda.gov
Ansell Perry de Mexico S.A. de C.V.Cd. Juarez Chihuahua, MexicoManufacturer0000api.fda.gov
Hill-Rom De Mexico S De RL De CVAPODACA Nuevo Leon, MexicoContract manufacturer0000api.fda.gov
Industrias Apson S.A de C.VAGUA PRIETA Sonora, MexicoContract manufacturer0000api.fda.gov
La Ada de AcunaCIUDAD DE ACUNA Coahuila, MexicoManufacturer0000api.fda.gov
Medtech Mexico Health, S. De R.L. De C.VSALINAS VICTORIA Nuevo Leon, MexicoManufacturer0000api.fda.gov
Medline Industries, LP - Mexicali (MXC)Mexicali Baja California, MexicoContract sterilizer, Manufacturer0000api.fda.gov
Merit Maquiladora Mexico, S. DE R.L. DE C.V.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
SOLVENTUM US LLC (Apodaca)Apodaca Nuevo Leon, MexicoContract manufacturer0000api.fda.gov
Tech Creations TorreonTorreon Coahuila, MexicoContract manufacturer0000api.fda.gov
Tri-State De Mexico, S. De R.L. De C.V.MEXICALI Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Wear Tex S. De R.L. De C.V.Torreon Coahuila, MexicoContract manufacturer, Exporter to the US0000api.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.