Data / Medical devices / Pad, Menstrual, Unscented / Mexico
FDA-registered makers of Pad, Menstrual, Unscented in Mexico: 9 establishments
9 establishments in Mexico are registered with the FDA to make Pad, Menstrual, Unscented (product code HHD). 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
- Pad, Menstrual, Unscented
- Product code
- HHD
- Country
- Mexico
Makers of Pad, Menstrual, Unscented in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Articulos Higienicos S.A. | Cuautitlan Izcalli Mexico, Mexico | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Enrocan Sapi De C.V. | Cuautitlan Izcalli Mexico, Mexico | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Essity Hygiene Y Salud Mexico, S.A. DE C.V. | Ecatepec, Mexico, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| K-C AFC Manufacturing, S. de R.L. de C.V | Nogales, Sonora Mexico, Mexico | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kimberly-Clark de Mexico | CUAUTITLAN Mexico, Mexico | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lambi, S.A. De C.V. | Escobedo Nuevo Leon, Mexico | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ontex Mexico Operations SA De CV | Tijuana Baja California, Mexico | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Procter & Gamble Manufacturing Mexico S. De R.L. De C.V. | MUNIC. TEPEJI D. RIO Hidalgo, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Productos Internacionales MABE SA DE CV | Puebla, Mexico | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.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.