Data / Medical devices / Hemostatic Wound Dressing Without Thrombin Or Other Biologics / China
FDA-registered makers of Hemostatic Wound Dressing Without Thrombin Or Other Biologics in China: 7 establishments
7 establishments in China are registered with the FDA to make Hemostatic Wound Dressing Without Thrombin Or Other Biologics (product code QSY). 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
- Hemostatic Wound Dressing Without Thrombin Or Other Biologics
- Product code
- QSY
- Country
- China
Makers of Hemostatic Wound Dressing Without Thrombin Or Other Biologics in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hangzhou Zeo-Innov Life Technology Co., Ltd. | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 2 | May 2, 2023 | 0 | 0 | 0 | api.fda.gov |
| Bestreat Safety & First Aid Solution Co., Ltd | Wuhan Hubei, China | Manufacturer | 1 | September 1, 2023 | 0 | 0 | 0 | api.fda.gov |
| Huizhou Foryou Medical Devices Co.,ltd. | HuiZhou Guangdong, China | Manufacturer | 1 | May 23, 2012 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Newvalue Medical Products Co., Ltd. | Taizhou Jiangsu, China | Exporter to the US, Manufacturer | 1 | September 1, 2023 | 0 | 0 | 0 | api.fda.gov |
| Taizhou Xinkang Medical Materials Co., Ltd | Taizhou Jiangsu, China | Exporter to the US, Manufacturer, Repackager or relabeler | 1 | May 2, 2023 | 0 | 0 | 0 | api.fda.gov |
| Beijing Huan Qiu Li Kang Biotech Co., Ltd. | Beijing, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beijing Taikesiman Technology Development Co., LTD | Li Qiao Beijing, 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.