Skip to the page

Data / Medical devices / Container, Specimen, Non-Sterile / Mexico

FDA-registered makers of Container, Specimen, Non-Sterile in Mexico: 8 establishments

8 establishments in Mexico are registered with the FDA to make Container, Specimen, Non-Sterile (product code NNI). 0 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
Container, Specimen, Non-Sterile
Product code
NNI
Country
Mexico

Makers of Container, Specimen, Non-Sterile in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Brady Mexico, S. de R.L. de C.V.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Cardinal Health (Kenmex Medical Specialties)TIJUANA Baja California, MexicoManufacturer0000api.fda.gov
Laboratorios Scantibodies S.A. De C.V.TECATE Baja California, MexicoContract manufacturer0000api.fda.gov
Laboratorios Scantibodies, S.A. de C.V.Tijuana Baja California, MexicoContract manufacturer0000api.fda.gov
Miwo Technologies Mexico S De R.L. De C.V.Tepeji Hidalgo, MexicoManufacturer0000api.fda.gov
Productos Para El Cuidado De La SaludNOGALES Sonora, MexicoContract manufacturer0000api.fda.gov
Tri-State De Mexico, S. De R.L. De C.V.MEXICALI Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Thermo Fisher Scientific (Monterrey)Apodaca Nuevo Leon, 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.