JINHUA RUIDI VEHICLE INDUSTRY CO LTD

FDA Device Registration & Listing · ZHEJIANG Jiangsu, CN · Registration 3012538618

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3012538618
FEI Number
3012538618
Entity Name
JINHUA RUIDI VEHICLE INDUSTRY CO LTD
City/State/Country
ZHEJIANG Jiangsu, CN
Establishment Address
3566 ERHUAN SOUTH RD, ZHEJIANG Jiangsu 321061, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
JINHUA RUIDI VEHICLE INDUSTRY CO LTD (Owner Number: 10060958)
Owner / Operator Contact Address
3566 ERHUAN SOUTH RD, ZHEJIANG, CN-JS 321061, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AFISCOOTERS AFISCOOTERS AFISCOOTERS AFISCOOTERS AFISCOOTERS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2019-07-20
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2019-07-20
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2019-07-20
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2019-07-20
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2019-07-20

Official Correspondent

Alvin Ye

US Agent Details

Ofer Tsoran Business: AFIKIM ELECTRIC VEHICLES Email: ofert@afiscooters.com Phone: (646) 6883238

Related Public Records

Same Entity

JINHUA RUIDI VEHICLE INDUSTRY CO LTD
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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012538618. Last updated year: 2026. Please use registration number 3012538618 when referencing this establishment in official correspondence.
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