FDA Device Establishments · JSON-LD · Markdown
FEI 3016851379 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3016851379 |
|---|---|
| Owner / Operator | ARTHREX, INC. (#1220287) |
| Address | Amperestraat 9, Venlo Limburg, 5928 PE, NL |
| Mandatory US Agent | Arthrex Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MBI |
| Regulation § (21 CFR) | 888.3040 |
Source: openFDA. Public-domain (CC0).