# K110225: Angiodynamics, Inc. Venacure 1470 Laser

- Pathway: 510(k) (Traditional)
- Applicant: AngioDynamics, Inc.
- Decided: May 13, 2011 after 108 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: 2 generations back to K043046 (2005). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082225: 15W Ceralas D 1470NM Diode Laser, Model D1470, Biolitec, Inc. (2008) Summary page 1.

## Cited in the summary but kept off the family tree
- K051995: Profemur Renaissance Hip Stem, Wrightmedicaltechnologyinc (2005). Our reading of the summary gave K051995, FDA’s number for Profemur Renaissance Hip Stem (Wrightmedicaltechnologyinc). Its FDA name has none of the distinctive words the summary uses for the device it names, “AngioDynamics Delta 15 and AngioDynamics Delta 30 Lasers”. Kept off the family tree.

## Indications for use
The AngioDynamics, VenaCure 1470 Laser is indicated 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/K110225
Methodology: https://510kreport.com/methodology