# K090744: CLARO

- Pathway: 510(k) (Traditional)
- Applicant: Clrs Technology Corporation
- Decided: Apr 15, 2010 after 391 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: 10 generations back to K943450 (1995). 102 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 104 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080638: CLARO, Clrs Technology Corporation (2008) Summary page 1.
- K043377: ZENO, Tyrell, Inc. (2005) Summary page 1.
- K060653: Thermaclear, Dermacare, Inc. (2006) Summary page 1.
- K080591: Tanda Skincare System, Model: Ptscs, Pharos Life Corporation (2008) Summary page 1.
- K081307: Omnilux Clear-U, Photo Therapeutics, Inc. (2009)

## Most influential descendants
- K150282: Shaser Skin Beauty Intense Pulsed Light System Family for Acne (2015), 0 descendants of its own

## Indications for use
The CLARO is indicated for the treatment of individual acne pimples in persons with mild to moderate inflammatory acne.

Source page: https://510kreport.com/device/K090744
Methodology: https://510kreport.com/methodology