Data / Medical devices / Choledochoscope And Accessories, Flexible/Rigid / China
FDA-registered makers of Choledochoscope And Accessories, Flexible/Rigid in China: 9 establishments
9 establishments in China are registered with the FDA to make Choledochoscope And Accessories, Flexible/Rigid (product code FBN). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Choledochoscope And Accessories, Flexible/Rigid
- Product code
- FBN
- Country
- China
Makers of Choledochoscope And Accessories, Flexible/Rigid 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 | 3 | April 3, 2026 | 0 | 0 | 0 | api.fda.gov |
| Micro-Tech (Nanjing) Co., Ltd. | NAN JING Jiangsu, China | Manufacturer | 3 | April 3, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Seegen Photoelectric Technology Co., Ltd | Shanghai, China | Manufacturer | 2 | March 7, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Seegen Photoelectric Technology Co., Ltd | Shanghai, China | Manufacturer | 2 | March 7, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Hugemed Medical Technical Development Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 2 | January 21, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shanghai AnQing Medical Instrument Co., Ltd | Shanghai, China | Manufacturer | 1 | October 17, 2023 | 0 | 0 | 0 | api.fda.gov |
| Zhuhai Pusen Medical Technology Co., Ltd. | Zhuhai Guangdong, China | Manufacturer | 1 | June 22, 2023 | 0 | 0 | 0 | api.fda.gov |
| Ningbo Wise Optomech Technology Corporation | Ningbo Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Besdata Technology Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.