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Levitate Technology ApS

DK-MF-000046389 · Denmark · Herlev

Levitate Technology ApS is registered in the European database on medical devices as a manufacturer, with 324 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa324

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerRegistered with FDA
Matched entryLEVITATE TECHNOLOGY APS (DK) · FDA 3019852058
Devices in EUDAMED324
Country of registrationDenmark

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