Establishment registration
NIHON KOHDEN AMERICA, INC.
FDA establishment registration 2080783 · Irvine, US
Key facts
| Registration number | 2080783 |
|---|---|
| Establishment name | NIHON KOHDEN AMERICA, INC. |
| Owner/operator | NIHON KOHDEN CORP. |
| Owner/operator number | 8030227 |
| FEI number | 2080783 |
| Address | 15353 Barranca Pkwy |
| City | Irvine |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | BXA, BZA, CBQ, CBR, CBS, CCK, CCL, CCW, DPS, DRG, DRQ, DRT, DSI, GWE, GWF, GWJ, GWQ, GXY, GYA, GYB, GYC, GZO, HPP, HXB, IKN, IKT, IOY, IZD, JJP, JXE and 19 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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