Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3035382637

FEI Number

3035382637

Entity Name

FEISHEN VIETNAM COMPANY LIMITED

City/State/Country

Ben Cat City Binh Duong, VN

Establishment Address

Factory C_1B_A1, DE4 Street, Lot C_1B_CN, My Phuoc 3 Industrial Park, Thoi Hoa Ward, Ben Cat City Binh Duong 820000, VN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

FEISHEN VIETNAM COMPANY LIMITED (Owner Number: 10092385)

Owner / Operator Contact Address

Factory C_1B_A1, DE4 Street, Lot C_1B_CN, My Phuoc 3 Industrial Park, Thoi Hoa Ward, Ben Cat City, VN-57 820000, VN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Edge 2 (KITASMB1940)

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	2024-12-31

Official Correspondent

Betty Zhou

US Agent Details

Richard Wittenberg Email: karen@troxusmobility.com Phone: (760) 9088999

Related Public Records

Same Entity

FEISHEN VIETNAM COMPANY LIMITED

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

View Entity Profile →

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035382637. Last updated year: 2026. Please use registration number 3035382637 when referencing this establishment in official correspondence.