Establishment registration
Arthrex GmbH
FDA establishment registration 3002579136 · Munich Bavaria, DE
Key facts
| Registration number | 3002579136 |
|---|---|
| Establishment name | Arthrex GmbH |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3002579136 |
| Address | Erwin-Hielscher-Strasse 9 |
| City | Munich Bavaria |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BWN, BZN, DXJ, FEI, FLE, FMF, FRG, FSM, FWB, FWL, FWZ, FZW, GAP, GAT, GAZ, GCJ, GEI, GFA, GFF, HAB, HRS, HRX, HSD, HST, HSX, HTD, HTJ, HTN, HTO, HTW and 35 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 1,000+ 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