Establishment registration
Instrumed GmbH dba Avalign German Specialty Instruments
FDA establishment registration 8010372 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010372 |
|---|---|
| Establishment name | Instrumed GmbH dba Avalign German Specialty Instruments |
| Owner/operator | Avalign Technologies |
| Owner/operator number | 10051835 |
| FEI number | 3007290840 |
| Address | 3 Unter Buchsteig |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | BWB, DWP, DWS, DXC, EHO, EMF, EMG, EMJ, EMM, EPY, FFO, FGN, FHQ, FHR, FTY, FZX, FZZ, GAD, GAF, GAH, GCJ, GDG, GDH, GDI, GDN, GDZ, GEA, GEG, GEI, GEN and 68 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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