Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033848208

FEI Number

3033848208

Entity Name

SHENZHEN TRIOUS MEDICAL TECHNOLOGY CO., LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Rm B102 Bldg B4 Rm 401 402 Bldg D3 YingZhan S T Estate Longtian Tongfuyu Rd 8, Longtian Com Longtian St Pingshan, Shenzhen Guangdong 518118, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Trious Medical Technology Co., Ltd (Owner Number: 10091653)

Owner / Operator Contact Address

Rm B102 Bldg B4, Rm 401 & 402 Bldg D3, YingZhan S&T Estate, Longtian Tongfuyu Rd #8;, Longtian Com, Longtian St, Pingshan, Shenzhen, CN-GD 518118, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K250448

PMA Number

N/A

All Registered Proprietary Names

Disposable Ureteral Access Sheath Disposable kidney stone retrieval basket Disposable non-vascular guide wire Disposable ureteral stent Disposable Percutaneous Nephrostomy Dilators

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FED	Endoscopic Access Overtube, Gastroenterology-Urology	Gastroenterology, Urology	Class 2	876.1500	2025-04-14
FFL	Dislodger, Stone, Basket, Ureteral, Metal	Gastroenterology, Urology	Class 2	876.4680	2024-10-22
OCY	Endoscopic Guidewire, Gastroenterology-Urology	Gastroenterology, Urology	Class 2	876.1500	2024-10-22
FAD	Stent, Ureteral	Gastroenterology, Urology	Class 2	876.4620	2025-05-27
LJE	Catheter, Nephrostomy	Unknown	Class U	N/A	2025-07-06

Official Correspondent

Yi Yingfang

US Agent Details

Qihui Zhang Business: ZYPPEL LLC Email: Qzhang@Zyppel.Com Phone: (617) 2991655

Related Public Records

Same Entity

Shenzhen Trious Medical Technology Co., Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K230752	FUJIFILM Healthcare Americas Corporation	Over-tube (TR-1208A); Over-tube (TR-1504A); Over-tube (TR-1507A)	2023-09-15

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0037-2023	Hobbs Medical, Inc.	2	Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001
Z-0038-2023	Hobbs Medical, Inc.	2	Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004
Z-0039-2023	Hobbs Medical, Inc.	2	Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023
Z-0040-2023	Hobbs Medical, Inc.	2	Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024
Z-0041-2023	Hobbs Medical, Inc.	2	Hobbs Biliary Pigtail Stent Kits (contains 3412) Catalog Number: 6027

Similar Registrations

Registration Number	Establishment Name	Location
3044858680	JIENO YOUCHENG MEDICAL TECHNOLOGY (SHANGHAI) CO., LTD.	Shanghai, CN
3030511423	ZHEJIANG YIGAO MEDICAL TECHNOLOGY CO., LTD.	Hangzhou Zhejiang, CN
3011050570	Gyrus ACMI, Inc.	Brooklyn Park, MN, US
3035480112	SEPLOU (ZHUHAI) CO.,LTD.	Zhuhai Guangdong, CN
3012345110	Novadaq Technologies ULC	Burnaby British Columbia, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033848208. Last updated year: 2026. Please use registration number 3033848208 when referencing this establishment in official correspondence.