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Data / Medical devices / Support, Patient Position / Mexico

FDA-registered makers of Support, Patient Position in Mexico: 13 establishments

13 establishments in Mexico are registered with the FDA to make Support, Patient Position (product code CCX). 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
Support, Patient Position
Product code
CCX
Country
Mexico

Makers of Support, Patient Position in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Boyd CorporationJuarez Chihuahua, MexicoContract manufacturer0000api.fda.gov
Dela De Mexico S De RL De CVTIJUANA Baja California, MexicoManufacturer0000api.fda.gov
Hill-Rom De Mexico S De RL De CVAPODACA Nuevo Leon, MexicoContract manufacturer0000api.fda.gov
Iimed Medical Mexicana S. De R.L. De C.V.Reynosa Tamaulipas, MexicoComplaint file establishment, Contract manufacturer0000api.fda.gov
Industrias Apson S.A de C.VAGUA PRIETA Sonora, MexicoContract manufacturer0000api.fda.gov
MAQ-OPS S. de R.L.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Merit Maquiladora Mexico, S. DE R.L. DE C.V.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Poliuretanos, S.A. De C.V.Toluca Mexico, MexicoContract manufacturer0000api.fda.gov
Productos Urologos De Mexico S.A. De C.V.MEXICALI Baja California, MexicoContract manufacturer0000api.fda.gov
Rogers Foam Juarez S de RL de CVJuarez Chihuahua, MexicoContract manufacturer0000api.fda.gov
Rogers Foam Tijuana S. de R.L. de C.V.Tijuana Baja California, MexicoContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Tri-State De Mexico, S. De R.L. De C.V.MEXICALI Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Velcromex, S.A. De C.V.AGUA PRIETA Sonora, 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.