Shenzhen Trious Medical Technology Co., Ltd.
Manufacturer and brand owner in Shenzhen, Guangdong, China. 6 device types, 8 products catalogued, 3 clearances.
Shenzhen Trious Medical Technology Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Stent, Ureteral, Catheter, Nephrostomy and 4 other device types. 7 of its products are catalogued under its own name. Its earliest product listing with the FDA dates from 2024.
Registration
| Registered name | SHENZHEN TRIOUS MEDICAL TECHNOLOGY CO., LTD |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3033848208 |
| FEI number | 3033848208 |
| DUNS | 698045520 |
| Establishment type | Manufacturer |
Chinese Registration
| Chinese legal name | 深圳泰睿仕医疗科技有限公司 |
|---|---|
| Unified social credit code | 91440300MA5F2DDH8Q |
| Source | export sales certificate, Guangdong medical products administration |
Location
| City | Shenzhen |
|---|---|
| Province | Guangdong |
| Address | Rm B102 Bldg B4 Rm 401 402 Bldg D3 YingZhan S T Estate Longtian Tongfuyu Rd 8 |
| Postal code | 518118 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Catheter, Nephrostomy | Class U | Disposable Percutaneous Nephrostomy Dilators | 2025 | 1 |
| Dislodger, Stone, Basket, Ureteral, Metal | Class 2 | Disposable kidney stone retrieval basket | 2024 | 21 |
| Endoscopic Access Overtube, Gastroenterology-Urology | Class 2 | Disposable Ureteral Access Sheath | 2025 | 19 |
| Endoscopic Guidewire, Gastroenterology-Urology | Class 2 | Disposable non-vascular guide wire | 2024 | 21 |
| Evacuator, Gastro-Urology | Class 2 | Negative pressure drainage device | 2025 | 5 |
| Stent, Ureteral | Class 2 | Disposable ureteral stent | 2025 | 4 |
Own-Brand Listings
Clearances
| Clearance | Decision date | Product code | Route | Held by |
|---|---|---|---|---|
| K250448 | 2025-07-03 | LJE | Traditional | This company |
| K243830 | 2025-05-14 | FAD | Traditional | This company |
| K243710 | 2025-04-11 | FED | Traditional | This company |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 2018 |
|---|---|
| Factory area | 7100 m² |
| Main products | ureteral stents, PCNL kits, guide wires, ureteral access sheaths |
| Certifications | ISO 13485, MDR, 510K, NMPA Registration |
| Export markets | 11 countries |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
The manufacturer named here can complete this record.