# K060787: Tattoostar Family

- Pathway: 510(k) (Special)
- Applicant: Asclepion Laser Technologies GmbH
- Decided: Sep 27, 2006 after 188 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.
78 later devices descend from it; 2 cite it directly.
0 of 79 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) RubyStar: named in the summary without a submission number

## Most influential descendants
- K073549: Q-Plus T (2008), 76 descendants of its own
- K140727: Cutera Picosecond Laser System (2014), 47 descendants of its own
- K153527: PicoWay Laser System (2016), 41 descendants of its own
- K123168: Q-Plus T+ Ipl Laser System (2012), 40 descendants of its own
- K130256: MDK Multi-Applications Platform (2013), 38 descendants of its own

## Indications for use
The TattooStar R is intended for use for cutting, vaporization and ablation of soft tissue and the removal of tattoos and benign pigment lesion. Some examples of pigment lesions are: Lentigines, Caf6-au-lait-blotches, Ephalides, BenignNaevi such as Naevus of Ota, Naevus of Ito, Epidermal Naevi, Congenital Naevi, Beckers Naevi, Blue Nevus, Naevus Spillus and Mongolian Spot.

Source page: https://510kreport.com/device/K060787
Methodology: https://510kreport.com/methodology