# Shenzhen Sino-K Medical Technology Co.,Ltd

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2020–2023): 3 510(k) clearances
- Product codes: DQA (1), FLL (1), DXQ (1)
- 510(k) review time since 2016: median 126 days, against 126 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- Orantech, Inc.: 1 (https://510kreport.com/company/orantech)
- Shenzhen Med-Link Electronics Tech Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-med-link-electronics-tech)
- Shenzhen Caremed Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-caremed-medical-technology)

## Firms that cite its devices most
- Avita Corporation: 1 (https://510kreport.com/company/avita)

## Its most-cited devices
- K231961: NIBPCuff (2023), cited by 1

## Recent decisions
- K231961: NIBPCuff (Aug 30, 2023)
- K223807: Reusable Temperature Probe, Disposable Temperature Probe (Aug 25, 2023)
- K192608: Disposable SpO2 Sensor (Jan 24, 2020)

Source page: https://510kreport.com/company/shenzhen-sino-k-medical-technology