Establishment registration
4190777 CANADA INC
FDA establishment registration 3011302631 · Saint-Laurent Quebec, CA
Key facts
| Registration number | 3011302631 |
|---|---|
| Establishment name | 4190777 CANADA INC |
| Owner/operator | 4190777 CANADA INC |
| Owner/operator number | 10047721 |
| FEI number | 3011302631 |
| Address | 4930 Chemin Bois-Franc |
| City | Saint-Laurent Quebec |
| Country | CA |
| Registration valid through | 2026 |
| Product codes listed | GEX |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database