ELECTRIC MOBILITY

FDA Device Registration & Listing · Cherry Hill, NJ, US · Registration 3038949386

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
3038949386
FEI Number
3038949386
Entity Name
ELECTRIC MOBILITY
City/State/Country
Cherry Hill, NJ, US
Establishment Address
1951 Old Cuthbert Rd Ste 204, Cherry Hill, NJ 08034, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Electric Mobility (Owner Number: 10095331)
Owner / Operator Contact Address
1951 OLD CUTHBERT RD, STE 204, Cherry Hill, NJ 08034, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K924515
PMA Number
N/A

All Registered Proprietary Names

VISTA VIPPI VEO SPORT VISTA VIPPI VEO SPORT

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 2026-02-26
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2026-02-26

Official Correspondent

Jordan Flowers

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Electric Mobility
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 3038949386. Last updated year: 2026. Please use registration number 3038949386 when referencing this establishment in official correspondence.
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