# K210823: LYMA Laser

- Pathway: 510(k) (Traditional)
- Applicant: Lyma Life, Ltd.
- Decided: Mar 18, 2022 after 364 days
- Product code: OHS (Light Based Over The Counter Wrinkle Reduction)
- 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: 3 generations back to K101190 (2010). 3 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120775: Light for Wrinkles, Led Intellectual Properties, LLC (2012) Summary page 4.
- K120560: Trinity Wrinkle Remover, Carol Cole Company (2012) Summary page 4.

## Most influential descendants
- K243330: LYMA Laser PRO (2025), 0 descendants of its own
- K233862: Nuna Lux (NUNL528) (2024), 0 descendants of its own

## Indications for use
The LYMA Laser is an Over-the-Counter (OTC) light based device intended for the use in treating full-face wrinkles.

Source page: https://510kreport.com/device/K210823
Methodology: https://510kreport.com/methodology