# K071451: Tattoostar Y

- Pathway: 510(k) (Special)
- Applicant: Asclepion Laser Technologies GmbH
- Decided: Aug 1, 2007 after 69 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.
9 later devices descend from it; 1 cites it directly.
0 of 10 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) Medlite CE: named in the summary without a submission number

## Most influential descendants
- K112669: Tattoostar Effect Y (2012), 8 descendants of its own
- K173692: D-Actor 200 Vibration Massage System (2018), 6 descendants of its own
- K210451: OrthoGold 100 (2021), 2 descendants of its own
- K220538: DolorClast Radial (2022), 1 descendant of its own
- K243488: Vmat Pro (2025), 0 descendants of its own

## Indications for use
The TattooStar Y is intended for use for incision, excision, ablation, vaporization of soft tissue for general dermatology and the removal of tattoos, the removal of benign pigmented lesion, the removal of vascular lesion and the removal of hair.

Source page: https://510kreport.com/device/K071451
Methodology: https://510kreport.com/methodology