# K140386: Lumina 24

- Pathway: 510(k) (Traditional)
- Applicant: Rogers Sciences, Inc.
- Decided: May 26, 2015 after 466 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: 10 generations back to K943450 (1995). 84 ancestors in all.
No later device cites it as a predicate yet.
0 of 85 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082247: Evis MD Platinum Red Light Therapy, Ageless Beauty Corporation (2008) Summary page 4.

## Indications for use
Intended to provide light to the body. Generally indicated to dermatology use for the treatment of benign superficial and pigmented lesions in patients with Fitzpatrick Skin Types II and III excluding vascular lesions such as hemangiomas, telangiectasia, and benign pigmented lesions such as solar lentigo, age spots, or freckles.

Source page: https://510kreport.com/device/K140386
Methodology: https://510kreport.com/methodology