# Guangzhou Sonostar Technologies Co., Ltd.

- Location (FDA's records): Guangzhou, CN
- FDA decisions: 3 (2017–2022): 3 510(k) clearances
- Product codes: IYN (2), IYO (1)
- 510(k) review time since 2016: median 169 days, against 83 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 6 (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
- Sonoscape Company Limited: 1 (https://510kreport.com/company/sonoscape)
- Healcerion Co., Ltd.: 1 (https://510kreport.com/company/healcerion)
- Penrith Corporation: 1 (https://510kreport.com/company/penrith)
- Mianyang Meike Electronic Equipment Co., Ltd.: 1 (https://510kreport.com/company/mianyang-meike-electronic-equipment)

## Firms that cite its devices most
- Bionet Co., Ltd.: 2 (https://510kreport.com/company/bionet)
- Mytech Intelligence (Shenzhen) Co., Ltd.: 2 (https://510kreport.com/company/mytech-intelligence-shenzhen)
- Suzhou Peaksonic Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/suzhou-peaksonic-medical-technology)

## Its most-cited devices
- K172750: Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe) (2018), cited by 4
- K171926: C5 Diagnostic Ultrasound System (2017), cited by 1
- K211321: Wireless Probe Type Ultrasound Scanner (Model: CProbe; Type: Type C, Type L, Type CT, Type CL) (2022), cited by 1

## Recent decisions
- K211321: Wireless Probe Type Ultrasound Scanner (Model: CProbe; Type: Type C, Type L, Type CT, Type CL) (Oct 13, 2022)
- K172750: Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe) (Feb 28, 2018)
- K171926: C5 Diagnostic Ultrasound System (Oct 27, 2017)

Source page: https://510kreport.com/company/guangzhou-sonostar-technologies