# K143007: Erchonia Zerona Z6 OTC

- Pathway: 510(k) (Traditional)
- Applicant: Erchonia Corporation
- Decided: Jan 15, 2015 after 87 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
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K202955: Contour Light CL-100 (2021), 8 descendants of its own
- K232977: Biophotas Celluma CONTOUR (2023), 5 descendants of its own
- K260129: Lumaflex Panel (ZLD-05, ZLD-05A, ZLD-05APro ) (2026), 1 descendant of its own
- K243854: Contour Light (CL-100) (2026), 1 descendant of its own
- K241947: EnergyLounger (TY-01) (2025), 1 descendant of its own

## Indications for use
The Zerona® Z6 OTC device is indicated for use as a non-invasive dermatological aesthetic treatment for the reduction of circumference of hips, waist, and thighs.

Source page: https://510kreport.com/device/K143007
Methodology: https://510kreport.com/methodology