Establishment registration
MEDTRONIC SOFAMOR DANEK USA, INC.
FDA establishment registration 3003120897 · Memphis, US
Key facts
| Registration number | 3003120897 |
|---|---|
| Establishment name | MEDTRONIC SOFAMOR DANEK USA, INC. |
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| FEI number | 3003120897 |
| Address | 4340 Swinnea Road |
| City | Memphis |
| State | TN |
| Country | US |
| Establishment types | Specification developer, Remanufacturer |
| Registration valid through | 2026 |
| Product codes listed | DXT, DXY, EQJ, ETN, EZW, FMF, FMH, FSM, FSZ, FTY, FZO, FZT, FZX, FZY, GAD, GDG, GDI, GEA, GEI, GET, GEY, GWF, GXD, GXI, GXZ, HAW, HBB, HBE, HRR, HRX and 92 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