Establishment registration
KLS Martin SE & Co. KG
FDA establishment registration 9610905 · Muhlheim/Donau Baden-Wurttemberg, DE
Key facts
| Registration number | 9610905 |
|---|---|
| Establishment name | KLS Martin SE & Co. KG |
| Owner/operator | KLS Martin SE & Co. KG |
| Owner/operator number | 10089006 |
| FEI number | 3002807464 |
| Address | Kolbinger StraBe 10 |
| City | Muhlheim/Donau Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, DZE, DZJ, DZL, DZN, EAX, ECP, ECS, EFL, EGN, EIG, EIX, EJB, EJY, EKB, EKC, EKR, ELE, EMF, EMG, EMI, EMJ, EMK, EML, EMM, EMN, EPY, FDG, FFO, FFQ and 137 more |
| Device classes | 1, 2 |
At a glance
- 100–999 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