Establishment registration
NUVASIVE, INC.
FDA establishment registration 2031966 · SAN DIEGO, US
Key facts
| Registration number | 2031966 |
|---|---|
| Establishment name | NUVASIVE, INC. |
| Owner/operator | NUVASIVE, INC. |
| Owner/operator number | 9036345 |
| FEI number | 3002980729 |
| Address | 7475 Lusk Blvd |
| City | SAN DIEGO |
| State | CA |
| Country | US |
| Establishment types | Export-only manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BSK, BTR, BXM, ETN, FST, FTL, FTY, GAD, GEI, GWF, HAW, HSB, HST, HTJ, HTW, HWA, HWB, HWJ, HWN, HWR, HWT, HXC, HXL, HXX, IKD, IKN, INK, JAA, JAC, KCT and 30 more |
| Device classes | 1, 2, 3, U |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 10–99 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