Establishment registration
Arthrex Manufacturing Inc.
FDA establishment registration 3015231789 · Pendleton, US
Key facts
| Registration number | 3015231789 |
|---|---|
| Establishment name | Arthrex Manufacturing Inc. |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3015231789 |
| Address | 130 Arthrex Drive |
| City | Pendleton |
| State | SC |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | BWN, CCX, EBW, EQH, FEI, FLE, FMF, FMP, FRG, FSM, FST, FTL, FXR, GAB, GAP, GAS, GAT, GBX, GCJ, GEI, GFA, GFF, HAB, HRS, HRX, HSB, HSD, HST, HSX, HTC and 54 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- 100–999 UDI devices (GUDID)
- Current Registration current
- None 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