Lilleborg AS
NO-MF-000012956 · Norway · Oslo
Lilleborg AS is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Devices declared under this manufacturer
- DekoRen+ Enzym
- DekoRen+ Mild
- DekoRen+ Spesial
- DekoRen+ Tørr
- DekoRen+ Ultra
- Dekoren+ Mild
Catalogue references include 3423, 3575, 3623, 3737, 3774, 3832.
European nomenclature codes declared: V0799.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Norway |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. Lilleborg AS was not found in either the U.S. or the Canadian register.