Data / Medical devices / Canada / Motion Composites
Motion Composites: FDA-registered device maker in St-Roch-de-lAchigan Quebec, Canada, 4 510(k) clearances
Motion Composites is registered with the FDA (registration 3011134213) in St-Roch-de-lAchigan Quebec, Canada. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated May 28, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011134213
- Address
- 160 Armand Majeau Sud, St-Roch-de-lAchigan Quebec, Canada, J0K3H0
- Owner or operator
- Motion Composites (10047250)
- Roles
- Manufacturer
- First device listed
- July 28, 2014
- Registered through
- 2026
- Brand names listed
- A6, A7, Apex Aluminum, Apex Carbon, Helio, Helio Kids A, Helio Kids C, Move and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cushion, Wheelchair | IMP | 1 | Manufacturer | accessdata.fda.gov |
| Support, Head And Trunk, Wheelchair | IMS | 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 |
|---|---|---|---|---|---|---|
| May 28, 2026 | K260295 | Helio Kids; Apex P | IOR | Substantially Equivalent | Motion Composites | accessdata.fda.gov |
| December 5, 2016 | K161425 | APEX Manual Wheelchair | IOR | Substantially Equivalent | Motion Composites | accessdata.fda.gov |
| May 1, 2015 | K143101 | Helio A7 Manual Wheelchair, Move Manual Wheelchair | IOR | Substantially Equivalent | Motion Composites | accessdata.fda.gov |
| December 19, 2012 | K120628 | HELIO | IOR | Substantially Equivalent | Motion Composites | accessdata.fda.gov |
Compare with other makers
- All makers of Wheelchair, Mechanical
- All makers of Support, Head And Trunk, Wheelchair
- All makers of Cushion, Wheelchair
Updated May 28, 2026. 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.