Establishment registration
Arthrex, Inc.
FDA establishment registration 3010331645 · Ave Maria, US
Key facts
| Registration number | 3010331645 |
|---|---|
| Establishment name | Arthrex, Inc. |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3010331645 |
| Address | 6875 Arthrex Commerce Drive |
| City | Ave Maria |
| State | FL |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | BWN, BZN, CCX, DXJ, EBW, EQH, FEI, FEM, FLE, FMF, FMP, FRG, FSM, FST, FTL, FWB, FWZ, FXR, FZW, GAB, GAP, GAS, GAT, GAZ, GBX, GCJ, GDZ, GEI, GEN, GFA and 74 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- None 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