Data / Medical devices / China / Yongkang Axios Industry And Trade Co.,ltd.
Yongkang Axios Industry And Trade Co.,ltd.: FDA-registered device maker in yongkang Zhejiang, China, 1 510(k) clearance
Yongkang Axios Industry And Trade Co.,ltd. is registered with the FDA (registration 3034989977) in yongkang Zhejiang, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 3, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3034989977
- Address
- No. 301,KeChuang Road, yongkang Zhejiang, China, 321399
- Owner or operator
- Yongkang Axios Industry and Trade Co.,Ltd. (10092308)
- Roles
- Manufacturer
- First device listed
- December 30, 2024
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | 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 |
|---|---|---|---|---|---|---|
| May 3, 2004 | K041025 | BUZZAROUND, VEHICLE, MOTORIZED 3-WHEELED | INI | Substantially Equivalent | Golden Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated May 3, 2004. 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.