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Data / Medical devices / Sleeve, Limb, Compressible / Mexico

FDA-registered makers of Sleeve, Limb, Compressible in Mexico: 6 establishments

6 establishments in Mexico are registered with the FDA to make Sleeve, Limb, Compressible (product code JOW). 5 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
Sleeve, Limb, Compressible
Product code
JOW
Country
Mexico

Makers of Sleeve, Limb, Compressible in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
DJ Orthopedics De Mexico, S.A. De C.V.TIJUANA Baja California, MexicoManufacturer, Remanufacturer, Repackager or relabeler8October 18, 2012000api.fda.gov
Stryker Tijuana OperationsTijuana Baja California, MexicoReprocessor3July 23, 2010000api.fda.gov
Cardinal Health (Kenmex Medical Specialties)TIJUANA Baja California, MexicoManufacturer2April 3, 2023000api.fda.gov
Convertors de Mexico S. de R.L. de C.VCD.JUAREZ Chihuahua, MexicoManufacturer1May 4, 2010000api.fda.gov
Tutamen De Mexico, LLCTijuana Baja California, MexicoManufacturer1April 1, 2016000api.fda.gov
Iimed Medical Mexicana S. De R.L. De C.V.Reynosa Tamaulipas, 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.