Data / Medical devices / Colonoscope And Accessories, Flexible/Rigid / China
FDA-registered makers of Colonoscope And Accessories, Flexible/Rigid in China: 10 establishments
10 establishments in China are registered with the FDA to make Colonoscope And Accessories, Flexible/Rigid (product code FDF). 5 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
- Colonoscope And Accessories, Flexible/Rigid
- Product code
- FDF
- Country
- China
Makers of Colonoscope And Accessories, Flexible/Rigid in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Guangzhou Red Pine Medical Instrument Co.,ltd. | Guangzhou Guangdong, China | Manufacturer | 1 | February 16, 2024 | 0 | 0 | 0 | api.fda.gov |
| Hangzhou AGS MedTech Co., Ltd. | Hangzhou Zhejiang, China | Manufacturer, Repackager or relabeler | 1 | April 6, 2022 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Seegen Photoelectric Technology Co., Ltd | Shanghai, China | Manufacturer | 1 | January 30, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Seegen Photoelectric Technology Co., Ltd | Shanghai, China | Manufacturer | 1 | January 30, 2026 | 0 | 0 | 0 | api.fda.gov |
| Yangzhou Fartley Medical Instrument Technology Co., Ltd | Yangzhou Jiangsu, China | Manufacturer | 1 | May 28, 2026 | 0 | 0 | 0 | api.fda.gov |
| Alton Shanghai Medical Instruments Co Ltd | Shanghai, China | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Daichuan Medical (Shenzhen) Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dalian Create Medical Products Co., LTD. | Dalian Liaoning, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sonoscape Medical Corp. | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sonoscape Medical Corp. | SHENZHEN Guangdong, China | Manufacturer | 0 | 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.