Data / Medical devices / Camera, Television, Endoscopic, Without Audio / China
FDA-registered makers of Camera, Television, Endoscopic, Without Audio in China: 6 establishments
6 establishments in China are registered with the FDA to make Camera, Television, Endoscopic, Without Audio (product code FWF). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Camera, Television, Endoscopic, Without Audio
- Product code
- FWF
- Country
- China
Makers of Camera, Television, Endoscopic, Without Audio in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anqing Changfan Medical Instrument Co., Ltd | Anqing Anhui, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anhui Shiyin Photoelectric Instrument Co., Ltd. | Suzhou Anhui, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangzhou T.K Medical Instrument Co., Ltd. | Guangzhou Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hunan Endoso Life Technology Co., Ltd | XiangTan Hunan, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tonglu Wanhe Medical Instrument Co., Ltd. | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xuzhou AKX Electronic Science and Technology Co., Ltd. | Xuzhou Jiangsu, 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.