# K261602: Eye Recovery Pro (PH-e03)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Goodwind Technology Development Co., Ltd.
- Decided: Aug 10, 2026 after 88 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: 16 generations back to K943450 (1995). 102 ancestors in all.
No later device cites it as a predicate yet.
0 of 103 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233556: LED Eye mask (EY-20R, A20, EY-20N), Shenzhen Kaiyan Medical Equipment Co., Ltd. (2024) Summary page 5.

## Indications for use
The Eye Recovery Pro (PH-e03) is an Over-the-Counter (OTC) device intended for use in treating wrinkles within the periorbital region.

Source page: https://510kreport.com/device/K261602
Methodology: https://510kreport.com/methodology