Sciton, Inc
Sciton, Inc holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2025.
Top product codes for Sciton, Inc
Recent clearances by Sciton, Inc
- K251077 — JOULE 1064nm System and Accessories
- K222958 — mJOULE RF System and Accessories
- K213761 — Joule diVa System
- K213350 — mJOULE System and Accessories
- K182173 — Joule System
- K180508 — JOULE SYSTEM
- K173285 — JOULE SYSTEM
- K122567 — JOULE 810/940/980 MULTI-PLATFORM SYSTEM
- K111483 — JOULE CLEARSENSE LASER SYSTEM
- K101916 — JOULE MULTI-PLATFORM SYSTEM
- K081352 — PROFILE MULTI-PLATFORM SYSTEM
- K070388 — PROFILE MULTI-PLATFORM SYSTEM
- K060033 — PROFILE MULTI-PLATFORM SYSTEM
- K040005 — PROFILE 2000/3000 LASER SYSTEM
- K032459 — PROFILE 1320 LASER SYSTEM
- K032460 — PROFILE BBL SYSTEM
- K023881 — PROFILE 1064 LASER SYSTEM
- K022466 — PROFILE 1320 LASER SYSTEM
- K022381 — PROFILE 1320 LASER SYSTEM
- K012552 — SCITON IMAGE HAIR REMOVAL LASER
- K010285 — CONTOUR PROFILE LASER
- K002853 — SCITON IMAGE HAIR REMOVAL LASER
- K003046 — IMAGE VASCULAR LASER
Data sourced from openFDA. This site is unofficial and independent of the FDA.