Naturelize GmbH
DE-MF-000005185 · Germany · Bad Emstal
Naturelize GmbH is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 10 |
|---|
Among these devices, 10 are declared sterile, 10 implantable.
Devices declared under this manufacturer
- Body Contour
- Body Intense
- Inline
- Inline Soft
- Inline soft pro
- Maxface
- Maxface soft
- Maxface soft pro
- Pearl
- Restore
Catalogue references include NAT-BC10, NAT-BI10, ZIL-0993, ZILS-0993, ZILS-0993PRO, ZMF-0964.
European nomenclature codes declared: P900402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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. Naturelize GmbH was not found in either the U.S. or the Canadian register.