Establishment registration
SILCOPLAST AG
FDA establishment registration 3013382619 · Wolfhalden Appenzell Ausserrhoden, CH
Key facts
| Registration number | 3013382619 |
|---|---|
| Establishment name | SILCOPLAST AG |
| Owner/operator | Silcoplast AG, Luchten 75, CH-9427 Wolfhalden |
| Owner/operator number | 10089547 |
| FEI number | 3013382619 |
| Address | LUCHTEN 75 |
| City | Wolfhalden Appenzell Ausserrhoden |
| Country | CH |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | HDR |
| Device classes | 2 |
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