# Shenzhen Coreray Technology, Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 4 (2018–2021): 4 510(k) clearances
- Names in FDA's records: Shenzhen Coreray Technology, Ltd. (3); Shenzhen Coreray Technology Co., Ltd. (1)
- Product codes: DSA (2), DXQ (1), DQA (1)
- 510(k) review time since 2016: median 230 days, against 141 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 5 (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
- Shenzhen Med-Link Electronics Tech Co., Ltd.: 2 (https://510kreport.com/company/shenzhen-med-link-electronics-tech)
- Orantech, Inc.: 1 (https://510kreport.com/company/orantech)
- Shenzhen Caremed Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-caremed-medical-technology)
- Solaris Medical Technology, Inc.: 1 (https://510kreport.com/company/solaris-medical-technology)

## Firms that cite its devices most
- Beijing Rongrui-Century Science & Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-rongrui-century-science-technology)

## Its most-cited devices
- K192404: Patient Monitoring Cable (SpO2 Extension Cable) (2020), cited by 1

## Recent decisions
- K211747: Reusable NIBP Cuff (Sep 23, 2021)
- K192404: Patient Monitoring Cable (SpO2 Extension Cable) (Jun 22, 2020)
- K173368: Reusable & Disposable SpO2 Sensors (Aug 31, 2018)
- K172797: ECG Cable/Leadwires (Feb 28, 2018)

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