Data / Medical devices / Clamp, Vascular / China
FDA-registered makers of Clamp, Vascular in China: 9 establishments
9 establishments in China are registered with the FDA to make Clamp, Vascular (product code DXC). 4 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
- Clamp, Vascular
- Product code
- DXC
- Country
- China
Makers of Clamp, Vascular in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Beijing Demax Medical Technology Co., Ltd. | Beijing, China | Manufacturer | 1 | January 4, 2023 | 0 | 0 | 0 | api.fda.gov |
| Lepu Medical Technology (beijing) Co., Ltd | Beijing, China | Manufacturer | 1 | October 23, 2014 | 0 | 0 | 0 | api.fda.gov |
| Lepu Medical Technology (beijing) Co., Ltd | Beijing, China | Manufacturer | 1 | October 23, 2014 | 0 | 0 | 0 | api.fda.gov |
| Sunny Medical Device (shenzhen) Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | March 16, 2020 | 0 | 0 | 0 | api.fda.gov |
| Shanghai INT Medical Instruments Co., Ltd. | Shanghai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Meccan Import and Export Corp. | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Terumo Medical Products (hangzhou) Co., Ltd. | HANGZHOU Zhejiang, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Demax Medical Technology Co., Ltd. | Tianjin, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. | Huizhou Guangdong, China | Contract 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.