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Data / Medical devices / Germany / LUNOR Aktiengesellschaft

LUNOR Aktiengesellschaft: FDA-registered device maker in Bad Liebenzell Baden-Wurttemberg, Germany, 1 510(k) clearance

LUNOR Aktiengesellschaft is registered with the FDA (registration 9680301) in Bad Liebenzell Baden-Wurttemberg, Germany. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 8, 1993. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9680301
FEI number
3005447474
Address
Lunor Allee 1, Bad Liebenzell Baden-Wurttemberg, Germany, 75378
Owner or operator
Lunor AG (10030562)
Roles
Contract manufacturer, Manufacturer
First device listed
October 19, 2009
Registered through
2026
Brand names listed
LUNOR, Lunor, Lunova

Devices it lists

DeviceProduct codeClassRoleSource
Frame, SpectacleHQZ1Contract manufacturer, Manufactureraccessdata.fda.gov
Sunglasses (Non-Prescription Including Photosensitive)HQY1Contract manufacturer, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 8, 1993K934301SPECTACLE FRAMESHQZSubstantially EquivalentGernot Lindner, Lunor-Vertriebaccessdata.fda.gov

Compare with other makers

Updated December 8, 1993. 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.