Data / Medical devices / China / Zhejiang Yigao Medical Technology Co., Ltd.
Zhejiang Yigao Medical Technology Co., Ltd.: FDA-registered device maker in Hangzhou Zhejiang, China, 1 510(k) clearance
Zhejiang Yigao Medical Technology Co., Ltd. is registered with the FDA (registration 3030511423) in Hangzhou Zhejiang, China. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 5, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3030511423
- Address
- No. 696, Fuxian Road Yinhu Street, Fuyang District Hangzhou, Zhejiang 311400 CHINA, Hangzhou Zhejiang, China, 311400
- Owner or operator
- Zhejiang YiGao Medical Technology Co., Ltd. (10091102)
- Roles
- Manufacturer
- First device listed
- October 17, 2024
- Registered through
- 2026
- Brand names listed
- Circular surgical stapler, Dispoable Stone Collector, Disposable Graduated Guidewire, Disposable Graduated Guidewire for Urological Treatments, Disposable Nitinol Urological Retrieval Coil, Disposable Stone Collector, Medical Endoscope Image Processor, Syfonix Suction Ureteral Access Sheath and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Catheter | KGZ | 1 | Manufacturer | accessdata.fda.gov |
| Collector, Urine, (And Accessories) For Indwelling Catheter | KNX | 2 | Manufacturer | accessdata.fda.gov |
| Dislodger, Stone, Basket, Ureteral, Metal | FFL | 2 | Manufacturer | accessdata.fda.gov |
| Endoscopic Access Overtube, Gastroenterology-Urology | FED | 2 | Manufacturer | accessdata.fda.gov |
| Endoscopic Guidewire, Gastroenterology-Urology | OCY | 2 | Manufacturer | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Manufacturer | accessdata.fda.gov |
| Stapler, Skin | QQS | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 5, 2025 | K250132 | Ureteral Access Sheath | FED | Substantially Equivalent | Zhejiang YiGao Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Endoscopic Access Overtube, Gastroenterology-Urology
- All makers of Collector, Urine, (And Accessories) For Indwelling Catheter
- All makers of Stapler, Skin
- All makers of Endoscopic Guidewire, Gastroenterology-Urology
- All makers of Dislodger, Stone, Basket, Ureteral, Metal
- All makers of Medical Device Data System
Updated September 5, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.