Establishment registration
Luxottica North Europe Ltd.
FDA establishment registration 3012297893 · St. Albans, Herts Hertfordshire, GB
Key facts
| Registration number | 3012297893 |
|---|---|
| Establishment name | Luxottica North Europe Ltd. |
| Owner/operator | Luxottica of America |
| Owner/operator number | 9032320 |
| FEI number | 3012297893 |
| Address | 2nd floor, Verulam Point |
| City | St. Albans, Herts Hertfordshire |
| Country | GB |
| Registration valid through | 2026 |
| Product codes listed | HOI, HQG, HQY, HQZ |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None 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