# K251288: Veincare

- Pathway: 510(k) (Special)
- Applicant: Wontech Co., Ltd.
- Decided: May 14, 2025 after 19 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: 4 generations back to K043046 (2005). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K241930: Veincare, Wontech Co., Ltd. (2024) Summary page 5.

## 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/K251288
Methodology: https://510kreport.com/methodology