Data / Medical devices / China / Guangdong Zhanyuan Smart Science and Technology Co. Ltd.
Guangdong Zhanyuan Smart Science and Technology Co. Ltd.: FDA-registered device maker in Dalang Town, Dongguan City Guangdong, China, 1 510(k) clearance
Guangdong Zhanyuan Smart Science and Technology Co. Ltd. is registered with the FDA (registration 3016733848) in Dalang Town, Dongguan City Guangdong, 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.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3016733848
- Address
- Room 301 Building 3, No. 60 Fumin South Road, Dalang Town, Dongguan City Guangdong, China, 523796
- Owner or operator
- Guangdong Zhanyuan Smart Science and Technology Co. Ltd (10064025)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- March 23, 2020
- Registered through
- 2026
- Brand names listed
- GB120A
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Contract manufacturer, 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.