Data / Medical devices / Container, I.V. / China
FDA-registered makers of Container, I.V. in China: 6 establishments
6 establishments in China are registered with the FDA to make Container, I.V. (product code KPE). 2 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
- Container, I.V.
- Product code
- KPE
- Country
- China
Makers of Container, I.V. in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Beijing L&Z Medical Technology Development Co., Ltd. | Beijing, China | Manufacturer | 2 | April 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Yangzhou Weideli Trading Co., Ltd. | Yangzhou Jiangsu, China | Specification developer | 1 | July 13, 2012 | 0 | 0 | 0 | api.fda.gov |
| Gri Medical & Electronic Technology Co., Ltd. | JIAXING Zhejiang, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ming Fai Industrial (shenzhen) Co. Ltd. | SHENZHEN Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wanying Health & Technology (Zhongshan) Co., Ltd. | Zhongshan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yangzhou Xingwei Medical Technology Co., LTD | Yangzhou City Jiangsu, 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.