Establishment registration
THE LINDEN GROUP CORP.
FDA establishment registration 3012336461 · Cedar Knolls, US
Key facts
| Registration number | 3012336461 |
|---|---|
| Establishment name | THE LINDEN GROUP CORP. |
| Owner/operator | The Linden Group Corp. |
| Owner/operator number | 9092461 |
| FEI number | 3012336461 |
| Address | 2B Wing Dr |
| City | Cedar Knolls |
| State | NJ |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | KQM |
| 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