# K130922: Erchonia Verju Laser System with Massager

- Pathway: 510(k) (Traditional)
- Applicant: Erchonia Medical, Inc.
- Decided: May 17, 2013 after 44 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K180338: Cellulize (2018), 2 descendants of its own
- K210535: UltraLight LED System (2021), 0 descendants of its own
- K202361: UltraSlim Digital, UltraSmooth Digital (2020), 0 descendants of its own

## Indications for use
The ERCHONIA® Verju® Laser System with Massager is indicated for use as a non-invasive dermatological aesthetic treatment as an adjunct for individuals intending to undergo liposuction procedures for the reduction of circumference of hips, waist and thighs. The Massager component is indicated for the temporary reduction in the appearance of cellulite.

Source page: https://510kreport.com/device/K130922
Methodology: https://510kreport.com/methodology