# K220729: The Luminance RED Acne Device

- Pathway: 510(k) (Traditional)
- Applicant: Luminance Medical Ventures, Inc.
- Decided: Jun 9, 2022 after 87 days
- Product code: OLP (Over-The-Counter Powered Light Based Laser For Acne)
- 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: 14 generations back to K943450 (1995). 104 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 106 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170260: BC-001+ Acne Purifier, Oriental Inspiration Limited (2017) Summary page 5.

## Most influential descendants
- K251843: Erchonia EVRL (2025), 0 descendants of its own

## Indications for use
The Luminance RED Acne Device is intended to emit energy in the red and blue region of the spectrum, and is specifically indicated to treat mild to moderate acne.

Source page: https://510kreport.com/device/K220729
Methodology: https://510kreport.com/methodology