Establishment registration
KLINGEL MEDICAL METAL GMBH
FDA establishment registration 3004370612 · Pforzheim Baden-Wurttemberg, DE
Key facts
| Registration number | 3004370612 |
|---|---|
| Establishment name | KLINGEL MEDICAL METAL GMBH |
| Owner/operator | Klingel medical metal GmbH |
| Owner/operator number | 10035920 |
| FEI number | 3004370612 |
| Address | Hanauer Str. 7 |
| City | Pforzheim Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | LXH, NHA |
| Device classes | 1, 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