Data / Medical devices / Canada / 5 Minds Mobility
5 Minds Mobility: FDA-registered device maker in Oshawa Ontario, Canada, 1 510(k) clearance
5 Minds Mobility is registered with the FDA (registration 3017171467) in Oshawa Ontario, Canada. It lists 11 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
- 3017171467
- Address
- 1597 Docking Court, Oshawa Ontario, Canada, L1K0H4
- Owner or operator
- 5 Minds Mobility (10071136)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- April 20, 2020
- Registered through
- 2026
- Brand names listed
- AD2, Acute, Align, Allay, Atlas Hybrid, Domus 1, Domus 3, Domus 4 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Exporter to the US | accessdata.fda.gov |
| Attachment, Commode, Wheelchair | INB | 1 | Exporter to the US | accessdata.fda.gov |
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Exporter to the US | accessdata.fda.gov |
| Bed, Therapeutic, Ac-Powered, Adjustable Home-Use | LLI | 2 | Exporter to the US | accessdata.fda.gov |
| Chair And Table, Medical | KMN | 1 | Exporter to the US | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Exporter to the US | accessdata.fda.gov |
| Cover, Mattress (Medical Purposes) | FMW | 1 | Manufacturer | accessdata.fda.gov |
| Cushion, Wheelchair | IMP | 1 | Exporter to the US | accessdata.fda.gov |
| Lift, Patient, Ac-Powered | FNG | 2 | Exporter to the US | accessdata.fda.gov |
| Mattress, Flotation Therapy, Non-Powered | IKY | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | Exporter to the US | 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 Cover, Mattress (Medical Purposes)
- All makers of Wheelchair, Mechanical
- All makers of Mattress, Flotation Therapy, Non-Powered
- All makers of Chair And Table, Medical
- All makers of Cushion, Wheelchair
- All makers of Bed, Ac-Powered Adjustable Hospital
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.