Vikta ApS
DK-MF-000044091 · Denmark · Ballerup
Vikta ApS is registered in the European database on medical devices as a manufacturer, with 51 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 51 |
|---|
Among these devices, 51 are declared active.
Devices declared under this manufacturer
- Flo-Form
- KomfiFlex Foam Mattress
- KomfiTilt ED.3 lateral tilt System
- KomfiTilt ED.5 lateral tilt
- KomfiTilt ED.6 lateral tilt
- KomfiTilt Go lateral tilt System
- PosiHeel
- PosiPerle
- PosiPillow
- PosiTilt
Showing 12 of 51 declared devices.
Catalogue references include FF1824, PP8012, PP8016, PP8035, PP8037, PP8051.
European nomenclature codes declared: V080302, V080701, V080702.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 51 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 51 |
|---|---|
| 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: Neither register. Vikta ApS was not found in either the U.S. or the Canadian register.