SUZHOU SWEETRICH VEHICLE INDUSTRY TECHNOLOGY CO,LTD.

FDA Device Registration & Listing · Suzhou Jiangsu, CN · Registration 3019984611

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
3019984611
FEI Number
3019984611
Entity Name
SUZHOU SWEETRICH VEHICLE INDUSTRY TECHNOLOGY CO,LTD.
City/State/Country
Suzhou Jiangsu, CN
Establishment Address
Building B, No.7 Chao Qian Road, Suzhou Industrial Zone, Suzhou Jiangsu 215123, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Suzhou Sweetrich Vehicle Industry Technology Co,Ltd. (Owner Number: 10086301)
Owner / Operator Contact Address
Building B, No.7 Chao Qian Road, Suzhou Industrial Zone, Suzhou, CN-JS 215123, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Mobility Aids Mobility Scooter (S1 SPORT, S1 PLUS, MAX SPORT, M1, PATRIOT) Mobility Scooter (Air Carbon) Mobility Scooter (Air Classic); Mobility Scooter (Air Traveller); Mobility Scooter (Air Traveller 2)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKX Aid, Transfer Physical Medicine Class 1 890.5050 2022-10-28
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2023-08-02
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2023-04-07
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2026-05-29
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2026-01-14

Official Correspondent

Ryan Chen

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Suzhou Sweetrich Vehicle Industry Technology 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 3019984611. Last updated year: 2026. Please use registration number 3019984611 when referencing this establishment in official correspondence.
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