# Shenzhen Goodwind Technology Development Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2022–2026): 3 510(k) clearances
- Product codes: OHS (2), OHT (1)
- 510(k) review time since 2016: median 88 days, against 88 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Light Tree Ventures Europe B.V.: 1 (https://510kreport.com/company/light-tree-ventures-europe)
- Shenzhen Idea Light Limited: 1 (https://510kreport.com/company/shenzhen-idea-light)
- Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-beauty-every-moment-intelligent-electric)
- Shenzhen Kaiyan Medical Equipment Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-kaiyan-medical-equipment)

## Firms that cite its devices most
- Shenzhen Leaflife Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-leaflife-technology)

## Its most-cited devices
- K222316: IPL Hair Removal Device (2022), cited by 1

## Recent decisions
- K261602: Eye Recovery Pro (PH-e03) (Aug 10, 2026)
- K252983: Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03) (Dec 17, 2025)
- K222316: IPL Hair Removal Device (Sep 28, 2022)

Source page: https://510kreport.com/company/shenzhen-goodwind-technology-development