# K042496: Adept Ultralite 532 Laser

- Pathway: 510(k) (Traditional)
- Applicant: Adept Medical Concepts
- Decided: Nov 2, 2004 after 49 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: 5 generations back to K933880 (1994). 15 ancestors in all.
23 later devices descend from it; 1 cites it directly.
0 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021975: Lasersystem Beautystar 532, Asclepion-Meditec AG (2002) Summary page 1.
- (no number) DioLite 532 laser: named in the summary without a submission number

## Most influential descendants
- K063396: Velure Family of Diode Lasers and Delivery Device Accessories (2007), 22 descendants of its own
- K100143: Pilot Diode Laser, Model 002-00139 (2010), 20 descendants of its own
- K123443: Precise SHP Diode Laser (2013), 9 descendants of its own
- K102036: Doctor Surgery Diode Lasers Family (2010), 7 descendants of its own
- K122567: Joule 810/940/980 Multi-Platform System (2013), 6 descendants of its own

## Indications for use
The ADEPT ULTRALITE 532 LASER is intended for vaporization and photocoagulation of vascular and pigmented lesions in soft tissue. Examples include: Telangiectasia Spider Naevi Angioma Hemangioma Leg veins (small, superficial - see above) Epidermal Naevi Lentigines (solar and senile) Verrucae Vulgares (Warts) Cherry Angioma Port Wine Stain

Source page: https://510kreport.com/device/K042496
Methodology: https://510kreport.com/methodology