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Laboratorios Liconsa, S.A.

Spain ES-MF-000009023 Last updated 17 Sep 2026

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Devices
6
Registries
EUDAMED
FDA recalls
0

Catalogue6

  • Gelifend Ref Vaginal Gel / Gel Vaginal 5 ml / 5 g

    Class IIb EUDAMED Active

  • Lactofeel Ref Vaginal Gel / Gel Vaginal 5 ml / 5 g

    Class IIb EUDAMED Active

  • Zonda Ref Dry powder inhalation device

    Class IIa EUDAMED Active

  • O-aplikator Ref Vaginal Ring Applicator

    Class I EUDAMED Active

  • Anette Aplicador Anel Vaginal Ref Vaginal Ring Applicator

    Class I EUDAMED Active

  • Ornibel Aplicador Ref Vaginal Ring Applicator

    Class I EUDAMED Active

What Laboratorios Liconsa, S.A. makes

Laboratorios Liconsa, S.A. manufactures topical and vaginal applicator devices, including gel formulations like Gelifend and Lactofeel, as well as applicators such as the O-aplikator, Anette Aplicador Anel Vaginal, and Ornibel Aplicador for localized medical applications.

The company’s portfolio includes devices classified as Class I, Class IIa, and Class IIb under EU regulations, all of which are registered in the EUDAMED database. The manufacturer is based in Spain.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Laboratorios Liconsa, S.A. manufacture?

Laboratorios Liconsa, S.A. specializes in topical and vaginal applicator devices. Their portfolio includes gel formulations like Gelifend and Lactofeel, which are designed for localized application, as well as applicators such as the O-aplikator, Anette Aplicador Anel Vaginal, and Ornibel Aplicador. These devices are intended for medical use in vaginal or topical administration.

Where is Laboratorios Liconsa, S.A. based?

Laboratorios Liconsa, S.A. is based in Spain. The company’s location in Spain aligns with its regulatory compliance requirements for manufacturing and distributing medical devices within the European market.

Which regulatory registries list Laboratorios Liconsa, S.A.’s devices?

Laboratorios Liconsa, S.A.’s devices are registered in the EUDAMED database, which is the European Union’s medical device registry. This database is used to track and provide transparency on medical devices authorized for use within the EU.

How are Laboratorios Liconsa, S.A.’s devices classified under EU regulations?

Laboratorios Liconsa, S.A.’s devices fall into three classification categories under EU regulations: Class I, Class IIa, and Class IIb. The classification determines the level of scrutiny and regulatory requirements for each device, with higher classes (e.g., Class IIb) typically involving more rigorous evaluation due to increased risk.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Spain
Address
S/N, c/ Dulcinea, Alcalá de Henares, Spain
Phone
+ 34 949 34 97 00
PRRC contact
Rubén Urbano
EUDAMED SRN
ES-MF-000009023