# K180888: LYFT

- Pathway: 510(k) (Traditional)
- Applicant: Uplevity, Inc.
- Decided: Aug 30, 2018 after 148 days
- Product code: OLP (Over-The-Counter Powered Light Based Laser For Acne)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K132833 (2014). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132833: Ultra Renew Plus, Accord Media (2014) Summary page 4.

## Indications for use
The LYFT device is intended to be used: LED functional mode To emit energy in the red and blue region of the spectrum, specifically to treat mild to moderate acne on the face. To emit energy in the red region of the spectrum for the treatment of periorbital wrinkles. Micro Vibration functional mode As an electrically powered device intended for medical purposes to relieve minor aches and pains.

Source page: https://510kreport.com/device/K180888
Methodology: https://510kreport.com/methodology