Establishment registration
Arthrex Mexico, S.A. de C.V.
FDA establishment registration 3011230048 · Col. Napoles Mexico, MX
Key facts
| Registration number | 3011230048 |
|---|---|
| Establishment name | Arthrex Mexico, S.A. de C.V. |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3011230048 |
| Address | Insurgentes Sur No. 859, Oficina 101 |
| City | Col. Napoles Mexico |
| Country | MX |
| Registration valid through | 2026 |
| Product codes listed | BWN, FMF, FMP, FWZ, GAP, GAT, GCJ, GEI, GFA, GFF, HRS, HRX, HST, HTJ, HTN, HTO, HTW, HTY, HTZ, HWC, HWE, HWT, HXB, HXD, HXJ, IZI, JDQ, JDR, JQC, KQM and 9 more |
| Device classes | 1, 2 |
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