Motion Composites
St-Roch-de-lAchigan Quebec, CA
MOTION COMPOSITES appears in FDA device records in St-Roch-de-lAchigan Quebec, CA. FDA records list 4 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 4 510(k) clearances for Motion Composites between 2012 and 2026. The busiest year on record is 2012, with 1. The most recent is 2026, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2012 | 1 |
| 2015 | 1 |
| 2016 | 1 |
| 2026 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K260295 | Helio Kids; Apex P | IOR | Substantially Equivalent | |
| K161425 | APEX Manual Wheelchair | IOR | Substantially Equivalent | |
| K143101 | Helio A7 Manual Wheelchair, Move Manual Wheelchair | IOR | Substantially Equivalent | |
| K120628 | HELIO | IOR | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3011134213 | 3011134213 | MOTION COMPOSITES | 160 Armand Majeau Sud, St-Roch-de-lAchigan Quebec J0K3H0 CA | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain