Data / Medical devices / Accessories, Photographic, For Endoscope (Exclude Light Sources) / China
FDA-registered makers of Accessories, Photographic, For Endoscope (Exclude Light Sources) in China: 8 establishments
8 establishments in China are registered with the FDA to make Accessories, Photographic, For Endoscope (Exclude Light Sources) (product code FEM). 0 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
- Accessories, Photographic, For Endoscope (Exclude Light Sources)
- Product code
- FEM
- Country
- China
Makers of Accessories, Photographic, For Endoscope (Exclude Light Sources) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anhui Shiyin Photoelectric Instrument Co., Ltd. | Suzhou Anhui, China | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beijing Fanxing Guangdian Medical Treatment Equipment Co Ltd | Beijing, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hunan Vathin Medical Instrument Co., Ltd. | Xiangtan Hunan, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Mole Electronic Technology Co., Ltd | Xuzhou Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qingdao O-Mec Medical Technology Co., Ltd. | Qingdao Shandong, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Besdata Technology Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Hugemed Medical Technical Development Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhongshan Wesee Meditech Co., Ltd. | Zhongshan 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.