# K062871: Lumacare LC-122M Non-Coherent Light Source

- Pathway: 510(k) (Traditional)
- Applicant: Lynton Lasers Limited
- Decided: Nov 14, 2006 after 50 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: 1 generation back to K031805 (2003). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031805: Blu-U, Model 4170, Dusa Pharmaceuticals, Inc. (2003) Summary page 1.

## Most influential descendants
- K100628: Plasmaluxls (2010), 0 descendants of its own

## Indications for use
The LumaCare LC-122M Non-coherent Light Source is intended to provide therapeutic light to the body The LumaCare LC-122M Non-coherent Light Source is generally indicated to treat dermatological conditions. The LumaCare LC-122M Non-coherent Light Source is specifically indicated to treat moderate inflammatory acne vulgaris.

Source page: https://510kreport.com/device/K062871
Methodology: https://510kreport.com/methodology