Data / Medical devices / Non-Surgical Gown / Mexico
FDA-registered makers of Non-Surgical Gown in Mexico: 10 establishments
10 establishments in Mexico are registered with the FDA to make Non-Surgical Gown (product code OEA). 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
- Non-Surgical Gown
- Product code
- OEA
- Country
- Mexico
Makers of Non-Surgical Gown in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ammar Apparel Ii S. De R.L De C.V. | CALKINI Campeche, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Grupo Alyger, S.A. De C.V. | Guadalupe Nuevo Leon, Mexico | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iimed Medical Mexicana S. De R.L. De C.V. | Reynosa Tamaulipas, Mexico | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Insumos Desechables Para La Salud S.A. De CV. | Tecoh Yucatan, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Industrias Apson S.A de C.V | AGUA PRIETA Sonora, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| La Ada De Acuna, S. de. R. L. de C. V. | COL.EDUCATIVA,NOGALES Sonora, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| La Ada de Acuna | CIUDAD DE ACUNA Coahuila, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solomed S.A. De C.V. | Zapopan Jalisco, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Tijuana Operations | Tijuana Baja California, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wear Tex S. De R.L. De C.V. | Torreon Coahuila, Mexico | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.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.