# K221444: LED Eye Perfector, model: EY-36A, EY-36B

- Pathway: 510(k) (Traditional)
- Applicant: Light Tree Ventures Europe B.V.
- Decided: Dec 8, 2022 after 204 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: 14 generations back to K943450 (1995). 100 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 104 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171386: dpl SpectraLite, Led Technologies, Inc. (2017) Summary page 5.
- K162489: RED Light Device, Zhongshan Bisen Plastic Electronic Products Co., Ltd. (2017) Summary page 5.

## Most influential descendants
- K233556: LED Eye mask (EY-20R, A20, EY-20N) (2024), 1 descendant of its own
- K261602: Eye Recovery Pro (PH-e03) (2026), 0 descendants of its own
- K251871: FEATHER 01 02 03 04 (Model:01) (2025), 0 descendants of its own

## Indications for use
The LED Eye Perfector (Model: EY-36A, EY-36B) is an Over-the-Counter (OTC) device intended for use in treating wrinkles within the periorbital region.

Source page: https://510kreport.com/device/K221444
Methodology: https://510kreport.com/methodology