Data / Medical devices / Australia / Magic Mobility
Magic Mobility: FDA-registered device maker in Scoresby Victoria, Australia, 6 510(k) clearances
Magic Mobility is registered with the FDA (registration 3003650116) in Scoresby Victoria, Australia. It lists 2 device types. The FDA files 6 510(k) clearances under its listings, the newest dated March 4, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003650116
- Address
- 3 International Court, Scoresby Victoria, Australia, 3179
- Owner or operator
- Magic Mobility (9034065)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- August 1, 2008
- Registered through
- 2026
- Brand names listed
- Extreme X8, Frontier, Frontier V4 FWD, Frontier V4 RWD, Frontier V6, Magic 360, Magic XT Series, Magic XT2 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Powered | ITI | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Wheelchair, Standup | IPL | 2 | Complaint file establishment, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 4, 2024 | K233877 | XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) | ITI | Substantially Equivalent | Magic Mobility | accessdata.fda.gov |
| November 19, 2021 | K213090 | Frontier Series Power Wheelchairs | ITI | Substantially Equivalent | Magic Mobility | accessdata.fda.gov |
| July 9, 2021 | K211574 | Extreme X8 | ITI | Substantially Equivalent | Magic Mobility | accessdata.fda.gov |
| March 17, 2021 | K203083 | Magic 360 Power Wheelchair | ITI | Substantially Equivalent | Magic Mobility | accessdata.fda.gov |
| April 10, 2009 | K090350 | EXTREME 4X4-X8 POWER WHEELCHAIR | ITI | Substantially Equivalent | Vestil Manufacturing Corp. | accessdata.fda.gov |
| April 4, 2003 | K030783 | FRONTIER MODEL X5 | ITI | Substantially Equivalent | Vestil Manufacturing Corp. | accessdata.fda.gov |
Compare with other makers
Updated March 4, 2024. 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.