Data / Medical devices / Catheter, Percutaneous / China
FDA-registered makers of Catheter, Percutaneous in China: 10 establishments
10 establishments in China are registered with the FDA to make Catheter, Percutaneous (product code DQY). 3 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
- Catheter, Percutaneous
- Product code
- DQY
- Country
- China
Makers of Catheter, Percutaneous in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| OrbusNeich Medical (Shenzhen) Co., Ltd. | SHENZHEN Guangdong, China | Complaint file establishment, Manufacturer | 4 | April 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Curatia Medical Limited | Suzhou Jiangsu, China | Manufacturer | 2 | December 14, 2018 | 0 | 0 | 0 | api.fda.gov |
| Lifetech Scientific (shenzhen) Co,.ltd | Shenzhen Guangdong, China | Manufacturer | 1 | February 14, 2011 | 0 | 0 | 0 | api.fda.gov |
| Covidien Medical Products (Shanghai) Manufacturing LLC | Shanghai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DK Medical Technology Co., Ltd. | Suzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Haolang Technology (foshan) Limited Corporation | Foshan Guangdong, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Circuit (Shanghai) Ltd. | Shanghai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Heartcare Medical Technology Corporation Limited | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Zenith Vascular Scitech Limited | Suzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Wallaby Medical Technologies CO., Inc. | Shanghai, China | Complaint file establishment, Contract manufacturer, 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.