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The Tracker / September 2026 / K262054

510(k) cleared

Electric Wheelchair

Yongkang Joymax Medical Technology Co., Ltd. · Sep 16, 2026 · K262054

FDA cleared the Electric Wheelchair from Yongkang Joymax Medical Technology Co., Ltd. on Sep 16, 2026 under K262054, a traditional 510(k). The device falls under product code ITI, Wheelchair, Powered, regulated at 21 CFR 890.3860 as a Class 2 device. The review panel was Physical Medicine.

FDA logged the submission as received on Jun 18, 2026. The decision came 90 days later, inside the 90 FDA-day goal for a 510(k).

This is the only decision on file for Yongkang Joymax Medical Technology Co., Ltd. in the last 12 months of the tracker.

Questions & Answers

What did FDA clear under K262054?

K262054 is the FDA 510(k) for Electric Wheelchair, submitted by Yongkang Joymax Medical Technology Co., Ltd.. FDA's decision date was Sep 16, 2026, under product code ITI (Wheelchair, Powered).

Who makes the Electric Wheelchair?

Yongkang Joymax Medical Technology Co., Ltd., based in Yongkang, is the applicant of record for K262054.

How long did the K262054 review take?

FDA received the submission on Jun 18, 2026 and issued its decision on Sep 16, 2026, 90 days later.

← All decisions in September 2026