# K133823: Nuface Mini Device

- Pathway: 510(k) (Abbreviated)
- Applicant: Carol Cole Company
- Decided: Apr 17, 2014 after 121 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: 3 generations back to K011935 (2001). 4 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103472: Nuface Plus, Carol Cole Company (2011) Summary page 1.

## Most influential descendants
- K152199: RejuvatoneMD (2016), 1 descendant of its own
- K260179: VITA Multi-Function Head Brush (TB-2343F, TB-2442F) (2026), 0 descendants of its own
- K182025: ClearUP Sinus Pain Relief (2019), 0 descendants of its own
- K171647: BeneLife Premium Facial Treatment Pack, Model: QZ0701A (2017), 0 descendants of its own

## Indications for use
The NuFACE®E Mini Facial Toning device is intended for facial stimulation and is indicated for over-the-counter cosmetic use (21I CFR 807 Subpart C).

Source page: https://510kreport.com/device/K133823
Methodology: https://510kreport.com/methodology