Medical Device Manufacturer · US , Mason , OH

The Procter & Gamble Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - The Procter & Gamble Co. Dental ✕

1 devices

1-1 of 1

Cleared Aug 28, 2009

VICKS POWERSHOT DRY THROAT & MOUTH RELIEF

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026