Establishment registration
TEKNO MEDICAL OPTIK-CHIRURGIE GMBH
FDA establishment registration 9611503 · TUTTLINGEN-Nendingen Baden-Wurttemberg, DE
Key facts
| Registration number | 9611503 |
|---|---|
| Establishment name | TEKNO MEDICAL OPTIK-CHIRURGIE GMBH |
| Owner/operator | TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH |
| Owner/operator number | 10027774 |
| FEI number | 3002808335 |
| Address | SATTLERSTRASSE 11 |
| City | TUTTLINGEN-Nendingen Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, EAJ, EAX, EBA, ECP, ECS, EFK, EFL, EGN, EHZ, EIC, EIG, EIR, EJE, EJG, EKB, EKC, EMF, EMG, EMH, EMI, EMJ, EMK, EMN, EPY, EQH, EWY, EZO, FAJ, FAS and 116 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 100–999 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