Data / Medical devices / Germany / LMT Medical Systems GMBH
LMT Medical Systems GMBH: FDA-registered device maker in Lubeck Schleswig-Holstein, Germany, 4 510(k) clearances
LMT Medical Systems GMBH is registered with the FDA (registration 3009514037) in Lubeck Schleswig-Holstein, Germany. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 26, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009514037
- Address
- Maria-Goeppert Str. 5, Lubeck Schleswig-Holstein, Germany, 23562
- Owner or operator
- LMT Medical Systems GmbH (10039265)
- Roles
- Complaint file establishment, Exporter to the US, Manufacturer
- First device listed
- December 21, 2011
- Registered through
- 2026
- Brand names listed
- LMT nomag IC 1.5, LMT nomag IC 3, NBAC 1.5T Flex, NBAC 1.5T Spine, NBAC 3T Flex, NBAC 3T Spine, NHAC 1.5T, NHAC 16 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Coil, Magnetic Resonance, Specialty | MOS | 2 | Complaint file establishment, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Incubator, Neonatal Transport | FPL | 2 | Complaint file establishment, Exporter to the US, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 26, 2017 | K171515 | NHAC 16 | MOS | Substantially Equivalent | Lmt Medical Systems GmbH | accessdata.fda.gov |
| August 18, 2010 | K091047 | NEONATE ARRAY COILS | MOS | Substantially Equivalent | Lmt Medical Systems GmbH | accessdata.fda.gov |
| July 31, 2006 | K062052 | LMT NOMAG IC 3.0 | FPL | Substantially Equivalent | Lmt Lammers Medical Technology GmbH | accessdata.fda.gov |
| November 21, 2003 | K033565 | LMT NOMAG IC 1,5 | FPL | Substantially Equivalent | Lmt Lammers Medical Technology GmbH | accessdata.fda.gov |
Compare with other makers
Updated July 26, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.