Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003820676

FEI Number

3003820676

Entity Name

FREERIDER, CORP.

City/State/Country

KAOHSIUNG, TW

Establishment Address

No. 22 Bengong 5th Road, GAN-SHAN Dist, KAOHSIUNG 820, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

FREERIDER, CORP. (Owner Number: 9030042)

Owner / Operator Contact Address

NO.22 BENGONG 5Th ROAD, GAN-SHAN DIST, KAOHSIUNG, TW-NOTA --820, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K160139

PMA Number

N/A

All Registered Proprietary Names

Crutch holder Seat Belt Luggie FR510-F Luggie Super Luggie Chair

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IMZ	Holder, Crutch And Cane, Wheelchair	Physical Medicine	Class 1	890.3910	2012-10-16
IML	Armrest, Wheelchair	Physical Medicine	Class 1	890.3920	2012-10-16
IQB	Belt, Wheelchair	Physical Medicine	Class 1	890.3920	2012-10-16
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2012-01-16
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	1999-10-29
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2015-09-15
KNN	Components, Wheelchair	Physical Medicine	Class 1	890.3920	2012-10-16
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2023-06-07

Official Correspondent

No official correspondent registered.

US Agent Details

ESTHER LIU Business: JS US REPRESENTATIVE OFFICE Email: us_agent@fdaclass.com Phone: (404) 9323207

Related Public Records

Same Entity

FREERIDER, CORP.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K853594	Vessa , Ltd.	VESSA FLIVVA	1985-09-24
K142783	Heartway Medical Products Co., Ltd.	HEARTWAY Electrically Powered Wheelchair P27	2015-06-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0036-2007	Medline Industries Inc	2	Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807600 - red and MDS807600B - blue
Z-0037-2007	Medline Industries Inc	2	Medline Strider Maxi 4 Scooter; a four wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807650 - red and MDS807650B - blue
Z-0005-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Z-0006-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
Z-0039-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors.

Similar Registrations

Registration Number	Establishment Name	Location
3035374295	ONLYCARE INC	Denver, CO, US
3014934217	CRADLE MEDICAL EQUIPMENT TECHNOLOGY CO.LTD	Foshan Guangdong, CN
3012251300	HANGZHOU ZHONGZHI INDUSTRY CO.,LTD	Hangzhou Zhejiang, CN
3007771912	Guangdong Marshell Electric Vehicle CO., LTD.	Zhaoqing Guangdong, CN
3004905643	NINGBO NINGYUAN IMPORT & EXPORT CO., LTD.	NINGBO, ZHEJIANG, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003820676. Last updated year: 2026. Please use registration number 3003820676 when referencing this establishment in official correspondence.