# K241930: Veincare

- Pathway: 510(k) (Traditional)
- Applicant: Wontech Co., Ltd.
- Decided: Nov 14, 2024 after 136 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: 3 generations back to K043046 (2005). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181632: Venacure 1470 Pro, Quanta System Spa (2018) Summary page 5.
- K160549: Medical Diode Laser Systems, Wuhan Gigaa Optronics Technology Co., Ltd. (2017) Summary page 6.

## Most influential descendants
- K251288: Veincare (2025), 0 descendants of its own

## Indications for use
Veincare is intended for use in the treatment of varicose veins and varicosities with superficial reflux of the Greater Saphenous Vein, and in the treatment of incompetent refluxing veins in the superficial venous system in the lower limb

Source page: https://510kreport.com/device/K241930
Methodology: https://510kreport.com/methodology