Establishment registration
KLS-Martin L.P.
FDA establishment registration 1057946 · Jacksonville, US
Key facts
| Registration number | 1057946 |
|---|---|
| Establishment name | KLS-Martin L.P. |
| Owner/operator | KLS Martin SE & Co. KG |
| Owner/operator number | 10089006 |
| FEI number | 1000525271 |
| Address | 11201 Saint Johns Industrial Pkwy S |
| City | Jacksonville |
| State | FL |
| Country | US |
| 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 127 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