SPARROW ROBOT, LLC

FDA Device Registration & Listing · Columbus, OH, US · Registration 3029926469

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
3029926469
FEI Number
3029926469
Entity Name
SPARROW ROBOT, LLC
City/State/Country
Columbus, OH, US
Establishment Address
4168 Fisher Road, Columbus, OH 43228, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Sparrow Robot, LLC (Owner Number: 10089122)
Owner / Operator Contact Address
4168 Fisher Road, Columbus, OH 43228, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K222711
PMA Number
N/A

All Registered Proprietary Names

ZiiLIF R5 Heavy Duty Mobility Scooter ZiiLIF S3 Folding Mobility Scooter ZiiLIF PC2 Folding Wheelchair ZiiLIF R3b Folding Mobility Scooter ZiiLIF X3 Folding Wheelchair ZiiLIF PC Folding Wheelchair

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 2023-11-07

Official Correspondent

Yuan Zheng

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sparrow Robot, LLC
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 3029926469. Last updated year: 2026. Please use registration number 3029926469 when referencing this establishment in official correspondence.
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