# K252146: Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003 SKB-2109,SKB-2129,SKB-2208PRO, SKB-2209)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Siken 3D Technology Development Co., Ltd.
- Decided: Dec 23, 2025 after 167 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K943450 (1995). 172 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 174 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K230506: PureLift Pro Edition, Xtreem Pulse (2023) Summary page 5.
- K243430: Micro-current Facial Beauty Device (AM-810B, AM-810W, AM-812B, AM-812W), Shenzhen Aozemei Technology Co., Ltd. (2024) Summary page 5.
- K233010: Beagank 4T Plus, Belega, Inc. (2023) Summary page 5.

## Most influential descendants
- K261370: LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA)) (2026), 0 descendants of its own

## Indications for use
Multi-functional Facial Beauty Device is a handheld portable device for over the counter aesthetic use including facial stimulation through MC(micro-current) mode.

Source page: https://510kreport.com/device/K252146
Methodology: https://510kreport.com/methodology