Data / Medical devices / China / Kingstar Medical (Xianning) Co., Ltd.
Kingstar Medical (Xianning) Co., Ltd.: FDA-registered device maker in Xianning City Hubei, China, 1 510(k) clearance
Kingstar Medical (Xianning) Co., Ltd. is registered with the FDA (registration 3013525704) in Xianning City Hubei, China. It lists 20 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 2, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013525704
- Address
- No. 79 Yong'andong Road Xian'an District, Xianning City Hubei, China, 437100
- Owner or operator
- WUHAN JACKY JENNY INDUSTRIES CO., LTD. (10040505)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- April 20, 2012
- Registered through
- 2026
- Brand names listed
- Alcohol pad, Cotton Balls, Cotton Rolls, Cotton With Gauze, Eye pad, Medical Dressng Kits, First Aid Kit with drug, Nonsterile Cotton Stick, Sterile cotton stick and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 2, 2023 | K232359 | Surgical face mask | FXX | Substantially Equivalent | Kingstar Medical (Xianning) Co., Ltd. | accessdata.fda.gov |
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Updated October 2, 2023. 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.