IERO Mobility Scooter (IERO-01)

FDA 510(k) K261232 · Jochu Technology Co., Ltd.

Substantially Equivalent

510(k) numberK261232

Submission

Device name
IERO Mobility Scooter (IERO-01)
Applicant
Jochu Technology Co., Ltd.
Hsin Chu, TW
Received
April 15, 2026
Decision date
July 14, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
INI – Vehicle, Motorized 3-Wheeled
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3800
Specialty
Physical Medicine

Other 510(k)s with product code INI

510(k)DeviceApplicantDecision
K260176Mobility Scooter (W3483, W3483A)INI · Traditional Zhejiang Innuovo Rehabilitation Devices Co.,Ltd08/10/2026SE
K260094Mobility Scooter (W3465, W3902 (S50 Carbon))INI · Traditional Zhejiang Innuovo Rehabilitation Devices Co.,Ltd08/10/2026SE
K261163Mobility Scooter (R200)INI · Traditional Yongkang Ruihe Metal Product Co., Ltd.07/07/2026SE
K253257Virgo Mobility Scooter (Virgo-D,Virgo-F)INI · Traditional Jiangsu Intco Medical Products Co., Ltd.06/08/2026SE
K253600Scooter (YD-03)INI · Traditional Yurob Rehabilitation Medical Co., Ltd.06/03/2026SE
K260717Mobility Scooter (Air Carbon)INI · Traditional Suzhou Sweetrich Vehicle Industry Technology…05/20/2026SE
K260237Mobility Scooter (X-12, X-14, X-17)INI · Traditional Wuyi Aichi Industry and Trade Co., Ltd.04/22/2026SE
K252813Electrical Scooter (SM4226)INI · Traditional Lerado Zhongshan Peaceful Cove Business Trading…03/17/2026SE
K253936Power Mobility Scooter (MJMA01, MJMA02)INI · Traditional Nanjing Mijo Technology Co., Ltd.03/12/2026SE
K253631Mobility Scooter (CL-Q3, CL-Q4)INI · Traditional Zhejiang Wei Ling New Energy Technology Co., Ltd.02/23/2026SE

Questions and answers

When was IERO Mobility Scooter (IERO-01) cleared by the FDA?

IERO Mobility Scooter (IERO-01) (K261232) received a 510(k) decision of Substantially Equivalent on July 14, 2026, 90 days after the submission was received.

What is the product code of K261232?

The FDA product code is INI – Vehicle, Motorized 3-Wheeled, a Class II (moderate risk) device regulated under 21 CFR 890.3800.