# K150336: Photonica Professional

- Pathway: 510(k) (Traditional)
- Applicant: Ward Photonics, LLC
- Decided: Feb 24, 2015 after 14 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K943450 (1995). 83 ancestors in all.
7 later devices descend from it; 2 cite it directly.
0 of 91 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030426: Omnilux Red, Photo Therapeutics Limited (2003) Summary page 4.

## Most influential descendants
- K160880: Photonica Professional (2016), 6 descendants of its own
- K180338: Cellulize (2018), 2 descendants of its own
- K192275: invisa-RED ELITE (2020), 1 descendant of its own
- K213534: PHantom Trilogy (2022), 0 descendants of its own
- K210535: UltraLight LED System (2021), 0 descendants of its own

## Indications for use
Photonica Professional is indicated for use in dermatology for the treatment of superficial, benign vascular, and pigmented lesions.

Source page: https://510kreport.com/device/K150336
Methodology: https://510kreport.com/methodology