Medical Device Manufacturer · US , Palo Alto , CA

Sciton, Inc - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 2000
23
Total
23
Cleared
0
Denied

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.

FDA 510(k) cleared devices by Sciton, Inc

23 devices
1-12 of 23
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