# Guangzhou Ekai Electronic Technology Co., Ltd.

- Location (FDA's records): Guangzhou, CN
- FDA decisions: 1 (2023–2023): 1 510(k) clearance
- Product codes: QAI (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (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
- Bellus Medical, LLC: 1 (https://510kreport.com/company/bellus-medical)

## Firms that cite its devices most
- Campomats S.R.L.: 1 (https://510kreport.com/company/campomats)
- Dermalogica, LLC: 1 (https://510kreport.com/company/dermalogica)
- Woorhi Mechatronics Co., Ltd.: 1 (https://510kreport.com/company/woorhi-mechatronics)

## Its most-cited devices
- K230420: Dr. pen Microneedling System (2023), cited by 3

## Recent decisions
- K230420: Dr. pen Microneedling System (Aug 11, 2023)

Source page: https://510kreport.com/company/guangzhou-ekai-electronic-technology