Establishment registration
ENDERS COLSMAN AG
FDA establishment registration 3016218280 · Werdohl North Rhine-Westphalia, DE
Key facts
| Registration number | 3016218280 |
|---|---|
| Establishment name | ENDERS COLSMAN AG |
| Owner/operator | Enders Colsman AG |
| Owner/operator number | 10061926 |
| FEI number | 3016218280 |
| Address | Brauck 1 |
| City | Werdohl North Rhine-Westphalia |
| Country | DE |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | FRG |
| Device classes | 2 |
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