Data / Medical devices / Guide, Wire, Catheter, Neurovasculature / China
FDA-registered makers of Guide, Wire, Catheter, Neurovasculature in China: 5 establishments
5 establishments in China are registered with the FDA to make Guide, Wire, Catheter, Neurovasculature (product code MOF). 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
- Guide, Wire, Catheter, Neurovasculature
- Product code
- MOF
- Country
- China
Makers of Guide, Wire, Catheter, Neurovasculature in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Deepintec Scientific Co., Ltd | Beijing, China | Manufacturer | 4 | March 19, 2026 | 0 | 0 | 0 | api.fda.gov |
| Enlight Medical Technologies (shenzhen) Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | November 18, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Achieva Medical Suzhou Co., Ltd. | Suzhou Jiangsu, China | Manufacturer | 1 | March 16, 2026 | 0 | 0 | 0 | api.fda.gov |
| Suzhou Zenith Vascular Scitech Limited | Suzhou Jiangsu, China | Manufacturer | 1 | April 16, 2026 | 0 | 0 | 0 | api.fda.gov |
| Terumo Medical Products (hangzhou) Co., Ltd. | HANGZHOU Zhejiang, China | Manufacturer | 1 | June 29, 2022 | 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.