Data / Medical devices / Nebulizer (Direct Patient Interface) / Mexico
FDA-registered makers of Nebulizer (Direct Patient Interface) in Mexico: 15 establishments
15 establishments in Mexico are registered with the FDA to make Nebulizer (Direct Patient Interface) (product code CAF). 11 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
- Nebulizer (Direct Patient Interface)
- Product code
- CAF
- Country
- Mexico
Makers of Nebulizer (Direct Patient Interface) in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Productos Urologos De Mexico S.A. De C.V. | MEXICALI Baja California, Mexico | Contract manufacturer, Manufacturer | 13 | May 17, 2017 | 0 | 0 | 0 | api.fda.gov |
| Rci Hudson De Mexico S. De RL. De CV. | Nuevo Laredo Tamaulipas, Mexico | Manufacturer | 12 | October 31, 2023 | 0 | 0 | 0 | api.fda.gov |
| Tecnologias Medicas Innovadoras S De RL | H. MATAMOROS Tamaulipas, Mexico | Manufacturer | 12 | January 23, 2020 | 0 | 0 | 0 | api.fda.gov |
| Salter Labs de Mexico de S.A. de C.V. | Chihuahua Mexico, Mexico | Contract manufacturer, Manufacturer, Repackager or relabeler | 7 | February 16, 2005 | 0 | 0 | 0 | api.fda.gov |
| ICU Medical Healthcare Manufacturing S.A. de C.V. | Tijuana, B.C. C.P. Baja California, Mexico | Manufacturer | 2 | October 25, 1993 | 0 | 0 | 0 | api.fda.gov |
| Westmed Javid de Mexico, S.A. de C.V. | NOGALES Sonora, Mexico | Manufacturer, Repackager or relabeler | 2 | February 3, 1993 | 0 | 0 | 0 | api.fda.gov |
| Baja Fur S.A. de C.V. | Tijuana Baja California, Mexico | Manufacturer, Repackager or relabeler | 1 | October 28, 2022 | 0 | 0 | 0 | api.fda.gov |
| Fisher & Paykel Healthcare S.a.de C.V. | Tijuana, Baja California, Mexico | Manufacturer | 1 | December 10, 2021 | 0 | 0 | 0 | api.fda.gov |
| ICU Medical Healthcare Manufacturing S.A. de C.V. | APODACA Nuevo Leon, Mexico | Manufacturer | 1 | September 10, 1990 | 0 | 0 | 0 | api.fda.gov |
| WESTMED de Mexico, S.A de C.V. | Tecate Baja California, Mexico | Manufacturer | 1 | February 3, 1993 | 0 | 0 | 0 | api.fda.gov |
| Westmed de Mexico, S.A de C.V | NOGALES Sonora, Mexico | Contract manufacturer, Manufacturer | 1 | March 25, 1980 | 0 | 0 | 0 | api.fda.gov |
| Flextronics Manufacturing Juarez S. DE R.L. DE C.V. | Juarez Chihuahua, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laboratorios PISA S.A. de C.V. | GUADALAJARA Jalisco, Mexico | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laboratorios PiSA, S. A. de C.V. | Tlajomulco de Zuniga Jalisco, Mexico | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Novem Medical S. De R.L. De C.V. | TIJUANA Baja California, Mexico | Contract manufacturer | 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.