Establishment registration
AOMORI OLYMPUS CO., LTD. Kuroishi Site
FDA establishment registration 9614641 · KUROISHI-SHI Aomori, JP
Key facts
| Registration number | 9614641 |
|---|---|
| Establishment name | AOMORI OLYMPUS CO., LTD. Kuroishi Site |
| Owner/operator | OLYMPUS CORPORATION |
| Owner/operator number | 9067818 |
| FEI number | 3003995201 |
| Address | 2-248-1 OKKONOKI |
| City | KUROISHI-SHI Aomori |
| Country | JP |
| Establishment types | Contract manufacturer, Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | BTG, EOB, EOQ, FAS, FBK, FBN, FCG, FDF, FDI, FDS, FDX, FED, FFL, FGE, FGX, GAA, GCJ, GEI, ITX, KGE, KNS, KTI, LFL, LQC, LQR, MND, MNL, NWW, OCZ, ODD and 5 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 1–9 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