Data / Medical devices / Endoscopic Video Imaging System/Component, Gastroenterology-Urology / China
FDA-registered makers of Endoscopic Video Imaging System/Component, Gastroenterology-Urology in China: 10 establishments
10 establishments in China are registered with the FDA to make Endoscopic Video Imaging System/Component, Gastroenterology-Urology (product code FET). 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
- Endoscopic Video Imaging System/Component, Gastroenterology-Urology
- Product code
- FET
- Country
- China
Makers of Endoscopic Video Imaging System/Component, Gastroenterology-Urology 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 7, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Seegen Photoelectric Technology Co., Ltd | Shanghai, China | Manufacturer | 1 | October 22, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Seegen Photoelectric Technology Co., Ltd | Shanghai, China | Manufacturer | 1 | October 22, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Sophway Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | July 1, 2025 | 0 | 0 | 0 | api.fda.gov |
| Zhuhai Pusen Medical Technology Co., Ltd. | Zhuhai Guangdong, China | Manufacturer | 1 | March 29, 2019 | 0 | 0 | 0 | api.fda.gov |
| Micro-Tech (Nanjing) Co., Ltd. | Nanjing Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Micro-Tech (Nanjing) Co., Ltd. | NAN JING Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qisda Electronics (suzhou) Co., Ltd. | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scivita Medical Technology Co., Ltd. | suzhou Jiangsu, 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 |
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.