Data / Medical devices / China / Dongguan Smarfody Mobility Technology CO.LTD.
Dongguan Smarfody Mobility Technology CO.LTD.: FDA-registered device maker in Dongguan Guangdong, China, 3 510(k) clearances
Dongguan Smarfody Mobility Technology CO.LTD. is registered with the FDA (registration 3020147377) in Dongguan Guangdong, China. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated January 29, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3020147377
- Address
- Room 101, No. 2 Xifu Street, Houjie Town, Dongguan Guangdong, China, 523940
- Owner or operator
- Dongguan Smarfody Mobility Technology CO.LTD. (10093501)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- May 27, 2025
- Registered through
- 2026
- Brand names listed
- Electric Scooter: Mojo-T580, Mojo-T500, Mojo-T550, Mojo-T580C, Mojo-T330, Mojo-T300, Mojo-T300C, Mojo-T360, Mojo-T330C, Mojo-T350, Mojo-T310, Mojo-T360C, Scooter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| January 29, 2026 | K252349 | Electric Scooter (Mojo-T330) | INI | Substantially Equivalent | Dongguan Smarfody Mobility Technology Co., Ltd. | accessdata.fda.gov |
| January 29, 2026 | K252347 | Electric Scooter (Mojo-T580) | INI | Substantially Equivalent | Dongguan Smarfody Mobility Technology Co., Ltd. | accessdata.fda.gov |
| June 24, 2019 | K182411 | Scooter, Model: R-100 | INI | Substantially Equivalent | Yongkang Dingchang Industry & Trade Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 29, 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.