Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015992762

FEI Number

3015992762

Entity Name

AFIKIM ELECTRIC VEHICLES USA INC

City/State/Country

Daytona Beach, FL, US

Establishment Address

1011 8TH STREET, SUITE 104, Daytona Beach, FL 32117, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

AFIKIM ELECTRIC VEHICLES USA INC (Owner Number: 10062160)

Owner / Operator Contact Address

1011 8TH STREET, SUITE 310, Daytona Beach, FL 32117, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K904522

PMA Number

N/A

All Registered Proprietary Names

AFIKIM ELECTRIC VEHICLES AFIKIM ELECTRIC VEHICLES AFIKIM ELECTRIC VEHICLES AFIKIM ELECTRIC VEHICLES AFIKIM ELECTRIC VEHICLES

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2023-12-21
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2023-12-21
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2023-12-21
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2023-12-21
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2023-12-21

Official Correspondent

Mr. Ofer Tsoran

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AFIKIM ELECTRIC VEHICLES USA INC

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-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.
Z-0040-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624Mini Power Wheel Chairs with internally threaded wheel mount motors.
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

Similar Registrations

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3002667030	TUNG KENG ENTERPRISE CO., LTD.	Taichung City, TW
3043165991	HEBEI DANSONG MEDICAL TECHNOLOGY CO., LTD.	SHIJIAZHUANG Hebei, CN
3036988603	SHENZHEN YATTLL INDUSTRY CO., LTD	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015992762. Last updated year: 2026. Please use registration number 3015992762 when referencing this establishment in official correspondence.