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Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / Mexico

FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in Mexico: 11 establishments

11 establishments in Mexico are registered with the FDA to make Lens, Spectacle, Non-Custom (Prescription) (product code HQG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Lens, Spectacle, Non-Custom (Prescription)
Product code
HQG
Country
Mexico

Makers of Lens, Spectacle, Non-Custom (Prescription) in Mexico

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Augen Opticos S.A.ENSENADA (EL SAUZAL) Baja California, MexicoManufacturer0000api.fda.gov
Carl Zeiss Vision Manufactura De Mexico, S. De R.LTIJUANA Baja California, MexicoManufacturer0000api.fda.gov
Centro Integral Optico, SA De CVMexico, MexicoManufacturer0000api.fda.gov
Costco Optical Laboratory #790Tepeji del Rio Hidalgo, MexicoManufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Essilor Tijuana Optica, S. De R.L. De C.V.Chihuahua, MexicoManufacturer0000api.fda.gov
EssilorLuxottica Mexico S. de R.L de C.VTijuana Baja California, MexicoContract manufacturer, Foreign private label distributor, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
IOTP-OB (Administradores de Maquila S de RL de CV)Municipio de Cajeme Sonora, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Sofi De Chihuahua10 Y 11, Chihuahua, Chib, MexicoManufacturer0000api.fda.gov
Sofi de Chihuahua SA de CVChihuahua, MexicoManufacturer0000api.fda.gov
Ymex (maquilas Teta Kawi, S.A. De C.V.)EMPALME Sonora, MexicoContract manufacturer, Manufacturer0000api.fda.gov
YMEX-OB (Administradores de Maquila S de RL de CV)Tramo Obregon-Navojoa Sonora, MexicoManufacturer0000api.fda.gov

Updated November 3, 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.