# K180338: Cellulize

- Pathway: 510(k) (Traditional)
- Applicant: Ward Photonics, LLC
- Decided: Sep 21, 2018 after 226 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: 11 generations back to K943450 (1995). 87 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 90 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130922: Erchonia Verju Laser System with Massager, Erchonia Medical, Inc. (2013) Summary page 5.
- K160880: Photonica Professional, Ward Photonics, LLC (2016) Summary page 5.

## Most influential descendants
- K210535: UltraLight LED System (2021), 0 descendants of its own
- K202361: UltraSlim Digital, UltraSmooth Digital (2020), 0 descendants of its own

## Indications for use
Cellulize® is indicated for use as a non-invasive dermatological aesthetic treatment 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/K180338
Methodology: https://510kreport.com/methodology