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Data / Medical devices / System, Nuclear Magnetic Resonance Imaging / Germany

FDA-registered makers of System, Nuclear Magnetic Resonance Imaging in Germany: 6 establishments

6 establishments in Germany are registered with the FDA to make System, Nuclear Magnetic Resonance Imaging (product code LNH). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
System, Nuclear Magnetic Resonance Imaging
Product code
LNH
Country
Germany

Makers of System, Nuclear Magnetic Resonance Imaging in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Siemens Healthineers AGERLANGEN Bavaria, GermanyComplaint file establishment, Contract manufacturer, Manufacturer82September 1, 2026000api.fda.gov
NORAS MRI products GMBHHOECHBERG Bavaria, GermanyContract manufacturer, Manufacturer2November 8, 2005000api.fda.gov
Neoscan Solutions GMBHMagdeburg Saxony-Anhalt, GermanyComplaint file establishment, Exporter to the US, Manufacturer1July 22, 2024000api.fda.gov
Northh Medical GMBHHamburg, GermanyManufacturer, Specification developer1February 4, 2022000api.fda.gov
Rapid Biomedical GMBHRIMPAR Bavaria, GermanyManufacturer1February 15, 2019000api.fda.gov
Siemens Healthineers AGFORCHHEIM Bavaria, GermanyComplaint file establishment, Manufacturer0000api.fda.gov

Updated November 2, 2026. 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.