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Data / Medical devices / Joint, Knee, External Brace / Mexico

FDA-registered makers of Joint, Knee, External Brace in Mexico: 14 establishments

14 establishments in Mexico are registered with the FDA to make Joint, Knee, External Brace (product code ITQ). 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
Joint, Knee, External Brace
Product code
ITQ
Country
Mexico

Makers of Joint, Knee, External Brace in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3M Edumex, S.A De C.VCD. JUAREZ Chihuahua, MexicoManufacturer0000api.fda.gov
Breg Mexico, S. De R.L. De C.V. (3)Mexicali Baja California, MexicoManufacturer0000api.fda.gov
Breg Mexico, S. De R.L. De C.V. (4)Mexicali Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
BSN Medical S.A. de C.V.Reynosa Tamaulipas, MexicoManufacturer0000api.fda.gov
Dela De Mexico S De RL De CVTIJUANA Baja California, MexicoManufacturer0000api.fda.gov
DJ Orthopedics De Mexico, S.A. De C.V.TIJUANA Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Medtech Acuna S.A. De C.V.Acuna Coahuila, MexicoContract manufacturer0000api.fda.gov
MFG AmpTijuana Baja California, MexicoManufacturer0000api.fda.gov
Moosni Internacional SA De CVHERMOSILLO Sonora, MexicoManufacturer0000api.fda.gov
Ossur MexicoTijuana Baja California, MexicoContract manufacturer0000api.fda.gov
SEI Medical S.A. de C.V.Juarez Chihuahua, MexicoContract manufacturer0000api.fda.gov
Tutamen De Mexico, LLCTijuana Baja California, MexicoManufacturer0000api.fda.gov
Viotin Trading Limited, S.A. De C.V.Mexico City Ciudad de Mexico, MexicoManufacturer0000api.fda.gov
Zeffer Research & Assoc. S. A. de C. V.Ensenada Baja California, MexicoContract manufacturer, 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.