LABORATOIRE DE CONTACTOLOGIE APPLIQUEE - LCA
FR-MF-000001732 · France · CHARTRES
LABORATOIRE DE CONTACTOLOGIE APPLIQUEE - LCA is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 16 |
|---|---|
| Class I | 12 |
| Class IIb | 7 |
Most frequent device types declared: ARTHRUM H 2%, ARTHRUM HCS, COXARTHRUM, IXIUM HCS, IXIUM NAHA 2%.
Among these devices, 35 are declared sterile, 10 implantable.
Devices declared under this manufacturer
- Aiguille péri-rétrobulbaire 25G
- Aiguille péri-rétrobulbaire 27G
- Aiguille péribulbaire 25G
- Aiguille rétrobulbaire 23G
- COXARTHRUM
- Canule d'irrigation Rycroft 27G
- Canule d'irrigation Rycroft 30G
- Canule d'irrigation pour solution viscoélastique 25G
- Canule d'irrigation pour solution viscoélastique 27G
- Canule à hydrodissection angulée 27G
- IXIUM HCS
- IXIUM NAHA 2%
Showing 12 of 35 declared devices.
Catalogue references include 101-3100, 211-0200, 214-0200, 300-0000, R1636C, R5011C.
European nomenclature codes declared: P900402, Q021101, Q02030301, Q02030206, A010599, A010504.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 35 |
|---|---|
| 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. LABORATOIRE DE CONTACTOLOGIE APPLIQUEE - LCA was not found in either the U.S. or the Canadian register.