meddevicedb.com FDA Device Reference

Electric Scooter (Mojo-T580)

K252347 Class II Traditional
Decision Date
2026-01-29
Sponsor / Applicant
Dongguan Smarfody Mobility Technology Co., Ltd.

Technical Specification

510(k) Submission ID K252347
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2026-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Scooter (Mojo-T580) received FDA 510(k) clearance under submission number K252347, sponsored by Dongguan Smarfody Mobility Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2026-01-29.

Classification & Regulation

This clearance is catalogued under FDA product code INI and 21 CFR 890.3800, within the Physical Medicine review panel as a Class II device.