Establishment registration
Arthrex Japan G.K. (Shinjuku)
FDA establishment registration 3012470322 · Shinjuku-ku Tokyo, JP
Key facts
| Registration number | 3012470322 |
|---|---|
| Establishment name | Arthrex Japan G.K. (Shinjuku) |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3012470322 |
| Address | Shinjuku NS BLDG 28F |
| City | Shinjuku-ku Tokyo |
| Country | JP |
| Registration valid through | 2026 |
| Product codes listed | FEI, FMF, FSM, FST, GAB, GAT, GCJ, GEI, GFA, HIF, HRS, HSD, HST, HTN, HWC, IZI, JDR, KNW, KWS, LLZ, LRY, LXH, LXI, MAI, MBI, MDM, NBH, ORG, OSV, PHX and 1 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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