Establishment registration
MANI, INC. (HANAOKA FACTORY)
FDA establishment registration 3004467019 · SHIOYA Tochigi, JP
Key facts
| Registration number | 3004467019 |
|---|---|
| Establishment name | MANI, INC. (HANAOKA FACTORY) |
| Owner/operator | MANI, INC. (HEAD OFFICE) |
| Owner/operator number | 8030343 |
| FEI number | 3004467019 |
| Address | 151 HANAOKA, OOAZA, TAKANEZAWA |
| City | SHIOYA Tochigi |
| Country | JP |
| Registration valid through | 2026 |
| Product codes listed | EKS, HNN |
| Device classes | 1 |
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