Electric Scooter (Mojo-T580)
K-Number: K252347 · 2026-01-29
Decision Date2026-01-29
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric Scooter (Mojo-T580) is a medical device manufactured by Dongguan Smarfody Mobility Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-01-29 under approval number K252347. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Electric Scooter (Mojo-T580)?
Electric Scooter (Mojo-T580) is a medical device that received FDA 510(k) clearance on 2026-01-29. It is manufactured by Dongguan Smarfody Mobility Technology Co., Ltd.. The 510(k) number is K252347.
When was Electric Scooter (Mojo-T580) approved by the FDA?
Electric Scooter (Mojo-T580) received FDA 510(k) clearance on 2026-01-29, under approval number K252347.
What company makes Electric Scooter (Mojo-T580)?
Electric Scooter (Mojo-T580) is manufactured by Dongguan Smarfody Mobility Technology Co., Ltd..
What is the FDA product code for Electric Scooter (Mojo-T580)?
The FDA product code for Electric Scooter (Mojo-T580) is INI.
Other Devices by Dongguan Smarfody Mobility Technology Co., Ltd.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.