Establishment registration
Arthrex (Shanghai) Co., Ltd.
FDA establishment registration 3014262693 · Shanghai, CN
Key facts
| Registration number | 3014262693 |
|---|---|
| Establishment name | Arthrex (Shanghai) Co., Ltd. |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3014262693 |
| Address | 2205-2208 Garden Square |
| City | Shanghai |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | FEI, FMF, FWB, GAP, GAT, GCJ, GEI, GFA, HRS, HRX, HSD, HST, HTJ, HTN, HTO, HTW, HTY, HWC, HWE, HWT, HXJ, IZI, JDQ, JDR, KWS, LLZ, LRY, LXH, LXI, MAI and 8 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