Establishment registration
NUTEK Orthopaedics, Inc
FDA establishment registration 3005893246 · Fort Lauderdale, US
Key facts
| Registration number | 3005893246 |
|---|---|
| Establishment name | NUTEK Orthopaedics, Inc |
| Owner/operator | NUTEK ORTHOPAEDICS, INC. |
| Owner/operator number | 9091870 |
| FEI number | 3005893246 |
| Address | 641 SW 3rd Ave |
| City | Fort Lauderdale |
| State | FL |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | JEC, KQZ, KTT, LXT |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 1–9 UDI devices (GUDID)
- Current Registration current
- 1–9 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