Establishment registration
MYKITA NORTH AMERICA
FDA establishment registration 3005516815 · West Orange, US
Key facts
| Registration number | 3005516815 |
|---|---|
| Establishment name | MYKITA NORTH AMERICA |
| Owner/operator | MYKITA North America |
| Owner/operator number | 10044968 |
| FEI number | 3005516815 |
| Address | 80 Main St Ste 200 |
| City | West Orange |
| State | NJ |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | 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