# K252574: Erchonia CLX (Model # CFL)

- Pathway: 510(k) (Traditional)
- Applicant: Erchonia Corporation
- Decided: Dec 15, 2025 after 123 days
- Product code: OLI (Fat Reducing Low Level Laser)
- Device class: 2
- Regulation: 21 CFR 878.5400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K123237 (2013). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192544: Erchonia Emerald, Erchonia Corporation (2020) Summary page 5.
- K243811: Erchonia Zerona® VZ8, Erchonia Corporation (2025) Summary page 5.

## Indications for use
The Erchonia CLX is indicated for use as a non-invasive dermatological aesthetic treatment for improving the appearance of submental fat.

Source page: https://510kreport.com/device/K252574
Methodology: https://510kreport.com/methodology