Cleared Traditional

Erchonia CLX (Model # CFL)

K252574 · Erchonia Corporation · General & Plastic Surgery
Dec 2025
Decision
123d
Days
Class 2
Risk

About This 510(k) Submission

K252574 is an FDA 510(k) clearance for the Erchonia CLX (Model # CFL), a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Erchonia Corporation (Fountain Inn, US). The FDA issued a Cleared decision on December 15, 2025, 123 days after receiving the submission on August 14, 2025. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K252574 FDA.gov
FDA Decision Cleared SESE
Date Received August 14, 2025
Decision Date December 15, 2025
Days to Decision 123 days
Submission Type Traditional
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