Establishment registration
FANDF CO., LTD. MEDICAL DEVICE DEPARTMENT
FDA establishment registration 3012057020 · Hachioji-shi Tokyo, JP
Key facts
| Registration number | 3012057020 |
|---|---|
| Establishment name | FANDF CO., LTD. MEDICAL DEVICE DEPARTMENT |
| Owner/operator | FandF Co., Ltd. Medical Device Department |
| Owner/operator number | 10082420 |
| FEI number | 3012057020 |
| Address | 2969-2 Ishikawa-machi |
| City | Hachioji-shi Tokyo |
| Country | JP |
| Registration valid through | 2026 |
| Product codes listed | JJE |
| 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