Sciton, Inc - FDA 510(k) Cleared Devices
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
Cleared
Dec 19, 2025
JOULE 1064nm System and Accessories
General & Plastic Surgery
255d
Cleared
Apr 23, 2024
mJOULE RF System and Accessories
General & Plastic Surgery
574d
Cleared
Jul 19, 2022
Joule diVa System
General & Plastic Surgery
230d
Cleared
Apr 15, 2022
mJOULE System and Accessories
General & Plastic Surgery
189d
Cleared
Mar 06, 2019
Joule System
General & Plastic Surgery
208d
Cleared
May 18, 2018
JOULE SYSTEM
General & Plastic Surgery
81d
Cleared
Jan 29, 2018
JOULE SYSTEM
General & Plastic Surgery
105d
Cleared
Jun 19, 2013
JOULE 810/940/980 MULTI-PLATFORM SYSTEM
General & Plastic Surgery
300d
Cleared
Dec 07, 2011
JOULE CLEARSENSE LASER SYSTEM
General & Plastic Surgery
190d
Cleared
Mar 18, 2011
JOULE MULTI-PLATFORM SYSTEM
General & Plastic Surgery
252d
Cleared
Oct 23, 2008
PROFILE MULTI-PLATFORM SYSTEM
General & Plastic Surgery
162d
Cleared
May 02, 2007
PROFILE MULTI-PLATFORM SYSTEM
General & Plastic Surgery
82d