Establishment registration
INTERFOCUS INC.
FDA establishment registration 3043515178 · Mountain View, US
Key facts
| Registration number | 3043515178 |
|---|---|
| Establishment name | INTERFOCUS INC. |
| Owner/operator | Interfocus Inc. |
| Owner/operator number | 10095183 |
| FEI number | 3043515178 |
| Address | 650 CASTRO STREET, STE 120-458 |
| City | Mountain View |
| State | CA |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | HGX |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 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