# K191672: NuFACE Mini Device

- Pathway: 510(k) (Traditional)
- Applicant: Carol Cole Company Dba Nuface
- Decided: Oct 15, 2019 after 113 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: 4 generations back to K011935 (2001). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181008: NuFACE Trinity, Carol Cole Company Dba Nuface (2018) Summary page 4.

## Most influential descendants
- K201680: NuFACE Mini Plus (2021), 0 descendants of its own

## Indications for use
The NuFACE Mini Device is intended for facial and neck stimulation and is indicated for over-the-counter cosmetic use.

Source page: https://510kreport.com/device/K191672
Methodology: https://510kreport.com/methodology