# K150077: SonicLift

- Pathway: 510(k) (Traditional)
- Applicant: Pretika Corporation
- Decided: Nov 25, 2015 after 315 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: 2 generations back to K011935 (2001). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072260: Nuface, Model NU-4003, Carol Cole Company (2007) Summary page 4.
- K944909: Wahl Fresh Face, Wahl Clipper Corp. (1995) Summary page 4.

## Indications for use
This device is intended for facial stimulation and is indicated for over-the-counter cosmetic use.

Source page: https://510kreport.com/device/K150077
Methodology: https://510kreport.com/methodology