# K073332: V-Raser Diode Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Hoya Conbio, Inc.
- Decided: Feb 14, 2008 after 79 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: 6 generations back to K922901 (1992). 26 ancestors in all.
No later device cites it as a predicate yet.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063384: Diodent Micro Dental Laser System, Models 810 and 980, Hoya Conbio, Inc. (2007) Summary page 1.
- K041930: Varilite Laser System, Iridex Corporation (2004) Summary page 1.

## Indications for use
The V-Raser is intended for Incision, excision, ablation, vaporization and coagulation of soft tissue. Treatment of vascular lesions.

Source page: https://510kreport.com/device/K073332
Methodology: https://510kreport.com/methodology