# Amemo, Inc.

- Location (FDA's records): Milpitas, CA
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: DQA (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Beijing Choice Electronic Technololgy Co., Ltd.: 1 (https://510kreport.com/company/beijing-choice-electronic-technololgy)

## Firms that cite its devices most
- Shenzhen Aeon Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-aeon-technology)
- Shenzhen Imdk Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-imdk-medical-technology)

## Its most-cited devices
- K153021: Fingertip Pulse Oximeter A310 (2016), cited by 2

## Recent decisions
- K153021: Fingertip Pulse Oximeter A310 (Nov 22, 2016)

Source page: https://510kreport.com/company/amemo