# K244004: Microcurrent Facial Device (CEC101, EE0101, EEI101)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Dachi Communication Co., Ltd.
- Decided: Jul 10, 2025 after 196 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: 6 generations back to K011935 (2001). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233010: Beagank 4T Plus, Belega, Inc. (2023) Summary page 5.
- K103031: BMR Face, Bio-Medical Research, Ltd. (2011) Summary page 5.

## Most influential descendants
- K252553: Facial & Body Beauty Device (INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507) (2025), 0 descendants of its own

## Indications for use
CEC101 and EE0101: Microcurrent Facial Device is intended for facial stimulation for over-the-counter aesthetic use. EEI101: Microcurrent Facial Device is intended for facial, neck and body skin stimulation for over-the-counter aesthetic use.

Source page: https://510kreport.com/device/K244004
Methodology: https://510kreport.com/methodology