# K162886: Deka Motus AX

- Pathway: 510(k) (Traditional)
- Applicant: El.En Electronic Engineering Spa
- Decided: Jun 19, 2017 after 245 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
Longest line of descent: 19 generations back to K943450 (1995). 254 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 256 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150516: Deka Synchro Repla:Y Family of Laser Systems, El.En Electronic Engineering Spa (2015) Summary page 4.

## Most influential descendants
- K223540: AvalancheLase Family (2023), 0 descendants of its own

## Indications for use
The DEKA Motus AX laser system is indicated for: Temporary hair reduction. Stable long-term or permanent hair reduction through selective targeting of melanin in hair follicles. Permanent hair reduction is defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regime, on all skin types (Fitzpatrick I – VI) including tanned skin. Treatment of benign pigmented lesions. Treatment of wrinkles. Photocoagulation of benign dermatological vascular lesions (such as port-wine stains, hemangiomas, telangiectasias).

Source page: https://510kreport.com/device/K162886
Methodology: https://510kreport.com/methodology