Data / Medical devices / Stents, Drains And Dilators For The Biliary Ducts / China
FDA-registered makers of Stents, Drains And Dilators For The Biliary Ducts in China: 8 establishments
8 establishments in China are registered with the FDA to make Stents, Drains And Dilators For The Biliary Ducts (product code FGE). 8 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stents, Drains And Dilators For The Biliary Ducts
- Product code
- FGE
- Country
- China
Makers of Stents, Drains And Dilators For The Biliary Ducts in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Micro-Tech (Nanjing) Co., Ltd. | Nanjing Jiangsu, China | Manufacturer | 4 | April 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Micro-Tech (Nanjing) Co., Ltd. | NAN JING Jiangsu, China | Manufacturer | 4 | April 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Canyon Medical Inc. | Nanjing Jiangsu, China | Manufacturer | 1 | September 18, 2026 | 0 | 0 | 0 | api.fda.gov |
| Dongguan TT Medical, Inc. | Dongguan Guangdong, China | Manufacturer | 1 | March 9, 2023 | 0 | 0 | 0 | api.fda.gov |
| Hangzhou AGS MedTech Co., Ltd. | Hangzhou Zhejiang, China | Manufacturer, Repackager or relabeler | 1 | June 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Vedkang Medical Science and Technology Co.,Ltd. | Changzhou Jiangsu, China | Manufacturer | 1 | February 15, 2024 | 0 | 0 | 0 | api.fda.gov |
| Leo Medical Co., Ltd. | Changzhou Jiangsu, China | Manufacturer | 1 | December 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Chuangxiang Medical Technology Co., Ltd. | Hangzhou Zhejiang, China | Manufacturer | 1 | March 6, 2026 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.