# K253002: SkinStylus SteriLock MicroSystem (MP1209SL)

- Pathway: 510(k) (Traditional)
- Applicant: Esthetic Medical, Inc.
- Decided: Feb 19, 2026 after 153 days
- Product code: QAI (Powered Microneedle Device)
- Device class: 2
- Regulation: 21 CFR 878.4430
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to DEN160029 (2018). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180778: Exceed Microneedling Device, Mt. Derm GmbH (2018) Summary page 5.

## Indications for use
The SkinStylus SteriLock® MicroSystem is a microneedling device and accessories intended to be used as a treatment to improve the appearance of periorbital wrinkles in Fitzpatrick skin types I, II, III, IV, V, and VI in adults aged 34 years or older.

Source page: https://510kreport.com/device/K253002
Methodology: https://510kreport.com/methodology