Establishment registration
NUVASCULAR INC.
FDA establishment registration 3030003849 · Irvine, US
Key facts
| Registration number | 3030003849 |
|---|---|
| Establishment name | NUVASCULAR INC. |
| Owner/operator | Nuvascular Inc. |
| Owner/operator number | 10091454 |
| FEI number | 3030003849 |
| Address | 141 Innovation Dr Ste 100 |
| City | Irvine |
| State | CA |
| Country | US |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | KRD |
| 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