Lutz GmbH & Co. KG
DE-MF-000038332 · Germany · Solingen
Lutz GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- LYNXERA LA35
- LYNXERA LN35
- LYNXERA LS35
- LYNXERA XA35
- LYNXERA XN35
- LYNXERA XS35
Catalogue references include 10074721, 10074722, 10074723, 10074846, 10074847, 10074848.
European nomenclature codes declared: V010302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. Lutz GmbH & Co. KG was not found in either the U.S. or the Canadian register.