# K060457: Quadrostar 532

- Pathway: 510(k) (Special)
- Applicant: Asclepion Laser Technologies GmbH
- Decided: Mar 20, 2006 after 26 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
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) BeautyStar 532: named in the summary without a submission number

## Most influential descendants
- K133297: Quadrostarprogreen, Quadrostarproyellow (2014), 4 descendants of its own
- K261094: YellowStar (2026), 0 descendants of its own
- K251432: Olo (2025), 0 descendants of its own
- K203054: FlexSys (2021), 0 descendants of its own
- K172198: 585 (2017), 0 descendants of its own

## Indications for use
The QuadroStar 532 Laser System is intended for vaporization and photocoagulation of vascular and pigmented lesions in soft tissue.

Source page: https://510kreport.com/device/K060457
Methodology: https://510kreport.com/methodology