Establishment registration
STRYKER LEIBINGER GMBH & CO. KG
FDA establishment registration 8010177 · FREIBURG Baden-Wurttemberg, DE
Key facts
| Registration number | 8010177 |
|---|---|
| Establishment name | STRYKER LEIBINGER GMBH & CO. KG |
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| FEI number | 3002821504 |
| Address | BOTZINGER STRASSE 39-41 |
| City | FREIBURG Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DMG, DZE, DZI, DZJ, DZL, EHO, ERL, EZX, FSM, FTD, FTL, FTM, FWP, FZO, FZX, GCX, GCY, GDY, GEA, GEI, GEN, GEY, GWO, GXD, GXI, GXP, GXR, HAO, HAW, HBE and 47 more |
| Device classes | 1, 2, 3, U |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 10–99 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