# K060455: Multistar

- 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.
No later device cites it as a predicate yet.
0 of 1 device 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) Multipulse: named in the summary without a submission number

## Indications for use
The MultiStar Laser System is intended for the coagulation, ablation, vaporization, incision, excision, cutting of soft tissue in plastic surgery, general surgery, oral surgery, ENT, gynecology and dermatology.

Source page: https://510kreport.com/device/K060455
Methodology: https://510kreport.com/methodology