# K260153: Q-Switched Nd: YAG Laser System (Glamor Q)

- Pathway: 510(k) (Traditional)
- Applicant: Nanjing Bestview Laser S&T Co., Ltd.
- Decided: Apr 20, 2026 after 90 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: 17 generations back to K943450 (1995). 241 ancestors in all.
No later device cites it as a predicate yet.
0 of 242 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K193464: ND:YAG Laser, Beijing Superlaser Technology Co., Ltd. (2020) Summary page 5.

## Indications for use
The Q-Switched Nd:YAG Laser System is indicated for the treatment of: benign cutaneous lesions, such as warts, scars, striae, and psoriasis; benign pigmented lesions, including lentigines, nevi, and birthmarks; and the removal of black and/or blue tattoos.

Source page: https://510kreport.com/device/K260153
Methodology: https://510kreport.com/methodology