Establishment registration
Kinetec SAS
FDA establishment registration 8020836 · Tournes Ardennes, FR
Key facts
| Registration number | 8020836 |
|---|---|
| Establishment name | Kinetec SAS |
| Owner/operator | Kinetec USA, Inc. |
| Owner/operator number | 10045573 |
| FEI number | 3006734242 |
| Address | Zone Industrielle de Tournes |
| City | Tournes Ardennes |
| Country | FR |
| Registration valid through | 2026 |
| Product codes listed | BXB, ION |
| Device classes | 1 |
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