Data / Medical devices / Canada / Power Plus Mobility Inc
Power Plus Mobility Inc: FDA-registered device maker in Guelph Ontario, Canada, 1 510(k) clearance
Power Plus Mobility Inc is registered with the FDA (registration 3023141620) in Guelph Ontario, Canada. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 28, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023141620
- Address
- 50 Malcolm Rd., Guelph Ontario, Canada, N1K1A9
- Owner or operator
- Power Plus Mobility Inc (10085356)
- Roles
- Manufacturer, Remanufacturer
- First device listed
- June 7, 2022
- Registered through
- 2026
- Brand names listed
- Horizon, Horizon Tilt, Seat Cushions and Backs, Super Tilt Plus, Wheelchair Accessories
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Manufacturer | accessdata.fda.gov |
| Chair, With Casters | INM | 1 | Manufacturer, Remanufacturer | accessdata.fda.gov |
| Cushion, Wheelchair | IMP | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | 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 |
|---|---|---|---|---|---|---|
| October 28, 2022 | K221435 | SUPERTILT PLUS (STP) | IOR | Substantially Equivalent | Power Plus Mobility | accessdata.fda.gov |
Compare with other makers
- All makers of Cushion, Wheelchair
- All makers of Accessories, Wheelchair
- All makers of Chair, With Casters
- All makers of Wheelchair, Mechanical
Updated October 28, 2022. 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.