Skip to the page

Data / Medical devices / Restraint, Protective / Mexico

FDA-registered makers of Restraint, Protective in Mexico: 8 establishments

8 establishments in Mexico are registered with the FDA to make Restraint, Protective (product code FMQ). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Restraint, Protective
Product code
FMQ
Country
Mexico

Makers of Restraint, Protective in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
DJ Orthopedics De Mexico, S.A. De C.V.TIJUANA Baja California, MexicoManufacturer, Repackager or relabeler14November 22, 1996000api.fda.gov
Tri-State De Mexico, S. De R.L. De C.V.MEXICALI Baja California, MexicoManufacturer1August 28, 2008000api.fda.gov
Ansell Perry de Mexico S.A. de C.V.Cd. Juarez Chihuahua, MexicoManufacturer0000api.fda.gov
Domico Med-Device, LLCLas palomas Guanajuato, MexicoContract manufacturer0000api.fda.gov
MAQ-OPS S. de R.L.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Posey, S. De R.L. De C.V.Tijuana Baja California, MexicoManufacturer0000api.fda.gov
Posey, S. de R.L. de C.V.Tijuana Baja California, MexicoManufacturer0000api.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.