Data / Medical devices / United States / Metro Mobility Usa LLC
Metro Mobility Usa LLC: FDA-registered device maker in Mineola, NY, United States, 3 510(k) clearances
Metro Mobility Usa LLC is registered with the FDA (registration 3026585646) in Mineola, NY, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 19, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3026585646
- Address
- 159 Liberty Ave, Mineola, NY, United States, 11501
- Owner or operator
- Metro Mobility USA LLC (10087406)
- Roles
- Specification developer
- First device listed
- March 27, 2024
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vehicle, Motorized 3-Wheeled | INI | 2 | Specification developer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| July 19, 2023 | K231472 | Mobility Scooter (S1 SPORT, S1 PLUS, MAX SPORT) | INI | Substantially Equivalent | Suzhou Sweetrich Vehicle Industry Technology Co., Ltd. | accessdata.fda.gov |
| January 18, 2022 | K212503 | HP458E Electrically Powered Wheelchair | ITI | Substantially Equivalent | Kunshan Hi-Fortune Health Products Co., Ltd. | accessdata.fda.gov |
| July 13, 2021 | K192739 | Electric Wheelchair [Models: JRWD6010/JRWD6012] | ITI | Substantially Equivalent | Jerry Medical Instrument (Shanghai) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 19, 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.