# K110355: Venx Revolution

- Pathway: 510(k) (Traditional)
- Applicant: Venx, LLC
- Decided: Apr 22, 2011 after 74 days
- Product code: GAH (Stylet, Surgical, General & Plastic Surgery)
- Device class: 1
- Regulation: 21 CFR 878.4800
- 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 K000932 (2000). 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)
- K000932: Arachnophlebectomy Needle, Advanced Medical Products, Inc. (2000) Summary page 1.

## Indications for use
The VENX REVOLUTION TM is a manual surgical instrument intended for use in the destruction of spider veins in the lower extremities of the body.

Source page: https://510kreport.com/device/K110355
Methodology: https://510kreport.com/methodology