# Shenzhen Aeon Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2017–2020): 3 510(k) clearances
- Product codes: DQA (2), FLL (1)
- 510(k) review time since 2016: median 183 days, against 158 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 5 (1 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
- Amemo, Inc.: 1 (https://510kreport.com/company/amemo)

## Firms that cite its devices most
- Guangdong Long Yao Electronic Technology Co., Ltd.: 1 (https://510kreport.com/company/guangdong-long-yao-electronic-technology)
- Zhuhai Linte Medical Instrument Co., Ltd.: 1 (https://510kreport.com/company/zhuhai-linte-medical-instrument)
- Shenzhen Viatom Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-viatom-technology)
- Shenzhen Calibeur Industries Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-calibeur-industries)

## Its most-cited devices
- K190869: Pulse Oximeter (2019), cited by 3
- K171578: Infrared thermometer (2017), cited by 1
- K200414: Pulse Oximeter (2020), cited by 1

## Recent decisions
- K200414: Pulse Oximeter (Sep 23, 2020)
- K190869: Pulse Oximeter (Sep 13, 2019)
- K171578: Infrared thermometer (Nov 30, 2017)

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