# Guangdong Prestige Technology Co., Ltd.

- Location (FDA's records): Dongguan, CN
- FDA decisions: 5 (2023–2025): 5 510(k) clearances
- Names in FDA's records: Guangdong Prestige Technology Co., Ltd. (4); Guangdong Prestige Technology Company Limited (1)
- Product codes: INI (4), ITI (1)
- 510(k) review time since 2016: median 167 days, against 123 for FDA's reviews in the same codes and years (2 of 5 faster)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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
- Dongguan Prestige Sporting Goods Co., Ltd.: 1 (https://510kreport.com/company/dongguan-prestige-sporting-goods)

## Recent decisions
- K252835: Electric Scooter (S202572J, S2060, M2089, S2050) (Dec 23, 2025)
- K240270: Electric wheelchair (S7018) (Aug 27, 2024)
- K240272: Electric Scooter (M2085, S2091) (Jul 16, 2024)
- K230001: Electric Scooter (Model: M2020) (Jul 5, 2023)
- K230615: Electric Scooter (Model: S3312) (May 5, 2023)

Source page: https://510kreport.com/company/guangdong-prestige-technology