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Procter & Gamble Co.

Also registered as Procter & Gamble, Procter & Gamble Mfg. Co., Procter & Gamble, Inc., The Procter & Gamble Co.

Country not established FDA establishment FEI 1523399

Devices
100
Registrations
FDA
FDA recalls
0

Catalogue100

Newest first, rows 1-50 of 100

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Rows 1-50 of 100

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Company details

FDA FEI number
1523399
Address
6280 Center Hill Ave, CINCINNATI, OH, 45224

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Procter & Gamble, Inc. BELLEVILLE Ontario · CA FEI 1000213912

Frequently asked questions

How many devices does PROCTER & GAMBLE CO. have in the registry?

The registry currently lists 100 devices for PROCTER & GAMBLE CO.. Devices recorded under merged duplicate company entries are counted once.

Which registries list PROCTER & GAMBLE CO.'s devices?

Among its 50 most recently registered devices, PROCTER & GAMBLE CO. has devices listed in FDA 510(k) (50 devices).

What risk classes do PROCTER & GAMBLE CO.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for PROCTER & GAMBLE CO.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from PROCTER & GAMBLE CO. in the registry?

The most recently registered devices listed for PROCTER & GAMBLE CO. include RELY TAMPON, UNSCENTED MENSTRUAL PAD, TAMPAX COMPAK PEARL PLASTIC APPLICATOR SCENTED AND UNSCENTED TAMPONS and ALWAYS SUPER MAXIPAD-SCENTED.

Which FDA establishments are linked to PROCTER & GAMBLE CO.?

1 FDA establishment is linked to PROCTER & GAMBLE CO. in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.