# Shenzhen Trious Medical Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2025–2025): 3 510(k) clearances
- Product codes: FAD (1), LJE (1), FED (1)
- 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
- Ureteral Stent Company: 1 (https://510kreport.com/company/ureteral-stent)
- Coloplast Corp.: 1 (https://510kreport.com/company/coloplast)
- Youcare Technology Co.,Ltd. (Wuhan): 1 (https://510kreport.com/company/youcare-technology-co-wuhan)

## Firms that cite its devices most
- Zhuhai Pusen Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/zhuhai-pusen-medical-technology)

## Its most-cited devices
- K243710: Disposable ureteral access sheath (2025), cited by 1

## Recent decisions
- K250448: Disposable Percutaneous Nephrostomy Dilatation Kit (Jul 3, 2025)
- K243830: Disposable ureteral stent (May 14, 2025)
- K243710: Disposable ureteral access sheath (Apr 11, 2025)

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