Establishment registration
KEISEI MEDICAL INDUSTRIAL CO., LTD.
FDA establishment registration 9611484 · BUNKYO-KU Tokyo, JP
Key facts
| Registration number | 9611484 |
|---|---|
| Establishment name | KEISEI MEDICAL INDUSTRIAL CO., LTD. |
| Owner/operator | KEISEI MEDICAL INDUSTRIAL CO., LTD. |
| Owner/operator number | 8031595 |
| FEI number | 3002807390 |
| Address | 19-6, HONGO SANCHOME |
| City | BUNKYO-KU Tokyo |
| Country | JP |
| Registration valid through | 2026 |
| Product codes listed | DXC, EPT, GAR, GFD, INX, KDC |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- None 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