# Viatom Technology Co., Ltd.

- Location (FDA's records): Nanshan, Shenzhen, CN
- FDA decisions: 1 (2015–2015): 1 510(k) clearance
- Product codes: MWI (1)
- Predicates its devices cite: 3 (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
- Guangdong Biolight Meditech Co., Ltd.: 1 (https://510kreport.com/company/guangdong-biolight-meditech)
- Dailycare Biomedical, Inc.: 1 (https://510kreport.com/company/dailycare-biomedical)
- Microlife Intellectual Property GmbH: 1 (https://510kreport.com/company/microlife-intellectual-property)

## Firms that cite its devices most
- Dynosense Corp.: 1 (https://510kreport.com/company/dynosense)
- Multisensor Diagnostics (Dba Aidar Health): 1 (https://510kreport.com/company/multisensor-diagnostics-dba-aidar-health)
- Shenzhen Viatom Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-viatom-technology)

## Its most-cited devices
- K150869: Checkme Pro Health Monitor (2015), cited by 3

## Recent decisions
- K150869: Checkme Pro Health Monitor (Dec 10, 2015)

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