# K133473: Iluminage Skin Smoothing Laser

- Pathway: 510(k) (Special)
- Applicant: Cynosure, Inc.
- Decided: Jan 15, 2014 after 64 days
- Product code: OHS (Light Based Over The Counter Wrinkle Reduction)
- 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 K111454 (2012). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111454: Iluminage Diode Laser, Cynosure, Inc. (2012)

## Indications for use
The Iluminage Skin Smoothing Laser is indicated for use in the treatment of periorbital and perioral wrinkles.

Source page: https://510kreport.com/device/K133473
Methodology: https://510kreport.com/methodology