# K221427: V-Laser

- Pathway: 510(k) (Special)
- Applicant: Wontech Co., Ltd.
- Decided: Aug 24, 2022 after 100 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: 23 generations back to K943450 (1995). 546 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 549 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183156: V-Laser, Wontech Co., Ltd. (2019) Summary page 5.

## Most influential descendants
- K231054: V-Laser (2023), 1 descendant of its own
- K251094: Alma Veil (2025), 0 descendants of its own

## Indications for use
The V-Laser laser system is intended for use in surgical and aesthetic applications in the medical specialties of dermatology and general and plastic surgery.

Source page: https://510kreport.com/device/K221427
Methodology: https://510kreport.com/methodology