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 IIa | 324 |
|---|
Devices declared under this manufacturer
- Blade 10'' AL C4.0 70-80kg
- Footshell Forever R25 Black - I.D. 230mm
- Footshell Forever R26 Beige - I.D. 230mm
- Footshell Traction R28 Black - I.D. 250mm
- Forever 6'' AL C1.0 0-50kg 210mm
- Forever 7'' TI C2.0 65-80kg 210mm
- Forever 7'' TI C3.0 95-110kg 210mm
- Forever LP AL C3.0 95-110kg 230mm
- Forever LP TI C3.0 95-110kg 250mm
- Forever LP TI C3.5 110-125kg 210mm
- Forever S TI C2.5 80-95kg 250mm
- Quick Change Base - Male - Male TI
Showing 12 of 324 declared devices.
Catalogue references include LTA000043, LTA000404, LTA000405, LTA007401, LTA100053, LTA100079.
European nomenclature codes declared: Y062499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LEVITATE TECHNOLOGY APS (DK) · FDA 3019852058 |
| Devices in EUDAMED | 324 |
| Country of registration | Denmark |
Device-level evidence
| Devices with a numeric GTIN | 324 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. Levitate Technology ApS is registered in the United States but was not found in the Canadian register.