Establishment registration
CODAN US CORP.
FDA establishment registration 2016945 · SANTA ANA, US
Key facts
| Registration number | 2016945 |
|---|---|
| Establishment name | CODAN US CORP. |
| Owner/operator | CODAN US Corporation |
| Owner/operator number | 8010060 |
| FEI number | 2016945 |
| Address | 3501 WEST SUNFLOWER AVE. |
| City | SANTA ANA |
| State | CA |
| Country | US |
| Establishment types | Remanufacturer |
| Registration valid through | 2026 |
| Product codes listed | FPA, GCX, KNT, LHI |
| Device classes | 2 |
At a glance
- 10–99 Device listings
- 1–9 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