Medical Device Manufacturer · US , Cincinnati , OH

The Procter & Gamble Company

5 submissions · 5 cleared · Since 2012

Total

Cleared

Denied

The Procter & Gamble Company — FDA 510(k) Submissions

The Procter & Gamble Company has submitted 5 FDA 510(k) premarket notifications since 2012, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tampon, Menstrual, Unscented, Saliva, Artificial, Toothbrush, Powered . Use the specialty filter in the sidebar to narrow results.

5 devices

1–5 of 5

Oral-B Dry Mouth Oral Rinse

K203567 · LFD Saliva, Artificial · Dental

Apr 2021 119d

Oral-B Dry Mouth Oral Rinse

K201277 · LFD Saliva, Artificial · Dental

Sep 2020 112d

Oral-B iO Test Drive Power Brush Trial Program Kit

K200881 · JEQ Toothbrush, Powered · Dental

Aug 2020 147d

TAMPAX M PLASTIC TAMPONS, UNSCENTED