Procter & Gamble is one of 4871 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Procter & Gamble - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Procter & Gamble has 2 FDA 510(k) cleared medical devices. Based in Mason, US.
Historical record: 2 cleared submissions from 2008 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Procter & Gamble Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Procter & Gamble
2 devices