Foreo, Inc. - FDA 510(k) Cleared Devices

Foreo, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Las Vegas, US.

Latest FDA clearance: Feb 2026. Active since 2016.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by DD Consulting as regulatory consultant.