Data / Medical devices / United States / Sparrow Robot, LLC
Sparrow Robot, LLC: FDA-registered device maker in Columbus, OH, United States, 1 510(k) clearance
Sparrow Robot, LLC is registered with the FDA (registration 3029926469) in Columbus, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 9, 2023. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3029926469
- Address
- 4168 Fisher Road, Columbus, OH, United States, 43228
- Owner or operator
- Sparrow Robot, LLC (10089122)
- Roles
- Repackager or relabeler
- First device listed
- November 7, 2023
- Registered through
- 2026
- Brand names listed
- ZiiLIF PC Folding Wheelchair, ZiiLIF PC2 Folding Wheelchair, ZiiLIF R3b Folding Mobility Scooter, ZiiLIF R5 Heavy Duty Mobility Scooter, ZiiLIF S3 Folding Mobility Scooter, ZiiLIF X3 Folding Wheelchair
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 9, 2023 | K222711 | HS186B Scooter | INI | Substantially Equivalent | Suzhou Master Machinery Manufacturing Co.,Ltd | accessdata.fda.gov |
Compare with other makers
Updated January 9, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.