Establishment registration
KLS MARTIN SE & CO. KG
FDA establishment registration 3036795921 · Fridingen Baden-Wurttemberg, DE
Key facts
| Registration number | 3036795921 |
|---|---|
| Establishment name | KLS MARTIN SE & CO. KG |
| Owner/operator | KLS Martin SE & Co. KG |
| Owner/operator number | 10089006 |
| FEI number | 3036795921 |
| Address | Wurttemberger Str. 23 |
| City | Fridingen Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, DZN, EAX, ECP, ECS, EFL, EGN, EIG, EIX, EJB, EJY, EKB, EKC, EKR, EMF, EMG, EMI, EMJ, EMK, EML, EMM, EMN, EPY, FDG, FFO, FFQ, FGM, FNY, FSM, FTY and 97 more |
| Device classes | 1 |
At a glance
- 100–999 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