# K171647: BeneLife Premium Facial Treatment Pack, Model: QZ0701A

- Pathway: 510(k) (Traditional)
- Applicant: Infinitus (China) Company, Ltd.
- Decided: Oct 23, 2017 after 140 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). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133823: Nuface Mini Device, Carol Cole Company (2014) Summary page 5.
- K132613: Sonilase Light Therapy Device, Biorenew Labs, LLC (2014) Summary page 5.
- K141308: Nutra Light Red, Nutra Luxe MD, LLC (2014) Summary page 5.

## Indications for use
The micro current stimulation mode is intended for facial stimulation and is indicated for over-the-counter cosmetic use. The red light treatment function is intended for the treatment of periorbital wrinkles.

Source page: https://510kreport.com/device/K171647
Methodology: https://510kreport.com/methodology