Establishment registration
LUNDELL MANUFACTURING CORP.
FDA establishment registration 3002900281 · Minneapolis, US
Key facts
| Registration number | 3002900281 |
|---|---|
| Establishment name | LUNDELL MANUFACTURING CORP. |
| Owner/operator | Lundell Manufacturing Corp. |
| Owner/operator number | 10051706 |
| FEI number | 3002900281 |
| Address | 2700 Ranchview Ln N |
| City | Minneapolis |
| State | MN |
| Country | US |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | CBL |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None 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