Sciton, Inc - FDA 510(k) Cleared Devices

Sciton, Inc has 23 FDA 510(k) cleared general & plastic surgery devices. Based in Palo Alto, US.

Latest FDA clearance: Dec 2025. Active since 2000.

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.

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