Data / Medical devices / Mexico / Procter & Gamble Manufacturing Mexico S. de R.L. de C.V.
Procter & Gamble Manufacturing Mexico S. de R.L. de C.V.: FDA-registered device maker in Estado de Mexico, C.P., Mexico, 1 510(k) clearance
Procter & Gamble Manufacturing Mexico S. de R.L. de C.V. is registered with the FDA (registration 9710651) in Estado de Mexico, C.P., Mexico. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 5, 2006. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 9710651
- FEI number
- 3001605950
- Address
- Calle Cuatro No. 4 Fraccionamiento Industrial Alce Blanco Naucalpan de Juarez, Estado de Mexico, C.P., Mexico, 53370
- Owner or operator
- Procter & Gamble (9915005)
- Roles
- Manufacturer
- First device listed
- March 27, 1997
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Floss, Dental | JES | 1 | Manufacturer | accessdata.fda.gov |
| Tip, Rubber, Oral Hygiene | JEW | 1 | Manufacturer | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Manufacturer | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 5, 2006 | K061351 | ORAL-B SONIC COMPLETE | JEQ | Substantially Equivalent | Braun GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Toothbrush, Powered
- All makers of Floss, Dental
- All makers of Tip, Rubber, Oral Hygiene
- All makers of Toothbrush, Manual
Updated June 5, 2006. 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.