Data / Medical devices / Tubes, Vials, Systems, Serum Separators, Blood Collection / China
FDA-registered makers of Tubes, Vials, Systems, Serum Separators, Blood Collection in China: 15 establishments
15 establishments in China are registered with the FDA to make Tubes, Vials, Systems, Serum Separators, Blood Collection (product code JKA). 9 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
- Tubes, Vials, Systems, Serum Separators, Blood Collection
- Product code
- JKA
- Country
- China
Makers of Tubes, Vials, Systems, Serum Separators, Blood Collection in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. | Taihu Anhui, China | Exporter to the US, Manufacturer | 4 | March 24, 2023 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Caina Medical Co., Ltd | Jiangyin Jiangsu, China | Manufacturer | 2 | March 7, 2024 | 0 | 0 | 0 | api.fda.gov |
| Guangzhou Improve Medical Instruments Co., Ltd. | Guangzhou Guangdong, China | Contract manufacturer, Manufacturer | 1 | July 12, 2010 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Kangbao Medical Equipment Co., Ltd | Yangzhou Jiangsu, China | Manufacturer | 1 | December 22, 2023 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Micsafe Medical Technology Co., Ltd | Yancheng Jiangsu, China | Manufacturer | 1 | November 4, 2021 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Rongye Technology Co.,ltd | Yangzhou Jiangsu, China | Manufacturer | 1 | October 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Promisemed Hangzhou Meditech Co.,ltd. | Hangzhou Zhejiang, China | Contract manufacturer, Exporter to the US, Manufacturer | 1 | June 4, 2025 | 0 | 0 | 0 | api.fda.gov |
| Yangzhou Medline Industry Co., Ltd. | Yangzhou Jiangsu, China | Manufacturer | 1 | July 7, 2023 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Kindly Medical Devices Co., Ltd | WENZHOU Zhejiang, China | Contract manufacturer, Contract sterilizer, Manufacturer | 1 | June 4, 2018 | 0 | 0 | 0 | api.fda.gov |
| Beilun Plastech Inc | Ningbo Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jumin Bio-Technologies, Co., Ltd | Fengxian District Shanghai, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sol-Kl (shanghai) Medical Products Company Limited | Shanghai, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Hanaco Medical Co.,ltd. | Tianjin, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Winner Medical (hunan) Co., Ltd. | Changde Hunan, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weihai Jierui Medical Products Co., Ltd. | WEIHAI Shandong, 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.