Establishment registration
Kerecis Minneapolis
FDA establishment registration 3031976582 · Minneapolis, US
Key facts
| Registration number | 3031976582 |
|---|---|
| Establishment name | Kerecis Minneapolis |
| Owner/operator | Kerecis ehf |
| Owner/operator number | 10045392 |
| FEI number | 3031976582 |
| Address | 1601 West River Road N |
| City | Minneapolis |
| State | MN |
| Country | US |
| Registration valid through | 2026 |
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