Cleared Special

Contour Light (CL-100)

K243854 · Contour Research, LLC · General & Plastic Surgery
Feb 2026
Decision
424d
Days
Class 2
Risk

About This 510(k) Submission

K243854 is an FDA 510(k) clearance for the Contour Light (CL-100), a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Contour Research, LLC (Reno, US). The FDA issued a Cleared decision on February 13, 2026, 424 days after receiving the submission on December 16, 2024. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K243854 FDA.gov
FDA Decision Cleared SESE
Date Received December 16, 2024
Decision Date February 13, 2026
Days to Decision 424 days
Submission Type Special
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OLI — Fat Reducing Low Level Laser
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.5400
Definition Non-invasive Reduction In Fat Layer For Body Contouring