Laboratorios Liconsa, S.A.
ES-MF-000009023 · Spain · Alcalá de Henares
Laboratorios Liconsa, S.A. is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIb | 2 |
|---|---|
| Class IIa | 4 |
Most frequent device types declared: Dry powder inhalation device, Vaginal Gel / Gel Vaginal 5 ml / 5 g, Vaginal Ring Applicator.
Devices declared under this manufacturer
- Anette Aplicador Anel Vaginal
- Gelifend
- Lactofeel
- O-aplikator
- Ornibel Aplicador
- Zonda
Catalogue references include Dry powder inhalation device, Vaginal Gel / Gel Vaginal 5 ml / 5 g, Vaginal Ring Applicator.
European nomenclature codes declared: A99.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | LABORATORIOS INDAS SA (ES) · FDA 3013152936 |
| Devices in EUDAMED | 6 |
| Country of registration | Spain |
⚠️ A similar name exists; we do not assert it is the same company — why.
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.