Data / Medical devices / China / Wenzhou Kangshun Medical Devices Co.,ltd.
Wenzhou Kangshun Medical Devices Co.,ltd.: FDA-registered device maker in Wenzhou City Zhejiang, China, 1 510(k) clearance
Wenzhou Kangshun Medical Devices Co.,ltd. is registered with the FDA (registration 3009154535) in Wenzhou City Zhejiang, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 28, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009154535
- Address
- No.706 Yanyun Road,Lingkun Street,Oujiangkou Industrial Cluster District, Wenzhou City Zhejiang, China, 325011
- Owner or operator
- Wenzhou Kangshun Medical Devices Co.,Ltd. (10089633)
- Roles
- Manufacturer
- First device listed
- December 23, 2023
- Registered through
- 2026
- Brand names listed
- ,Aneroid Sphygmomanometer with stethoscope, ANEROID SPHYGMOMANOMETER, Aneroid Sphygmomanometer,Aneroid Sphygmomanometer With Stethoscope, Aneroid Sphygmomanometer,Model:Ks-1222,Ks-1621,Ks-3201,Ks-2201,Ks-2203, Blood Pressure Cuff, Stethoscope Model:ks-2035,ks-2045,ks-2026,ks-2015,ks-2036,Aneroid Sphygmomanometer,Model:Ks-2201,ks-2021, hammer, stethoscope
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Manufacturer | accessdata.fda.gov |
| Hammer, Surgical | FZY | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Manufacturer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| June 28, 2023 | K230859 | Aneroid Sphygmomanometer | DXQ | Substantially Equivalent | Wenzhou Kangshun Medical Devices Co.,Ltd | accessdata.fda.gov |
Compare with other makers
Updated June 28, 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.