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

The Procter & Gamble Company has 5 FDA 510(k) cleared medical devices. Based in Cincinnati, US.

Last cleared in 2021. Active since 2012. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by The Procter & Gamble Company Filter by specialty or product code using the sidebar.

1 device has linked clinical trial registered on ClinicalTrials.gov.