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LABORATOIRES THEA

FR-MF-000001384 · France · CLERMONT FERRAND

LABORATOIRES THEA is registered in the European database on medical devices as a manufacturer, with 68 devices declared. It has a similarly named entry in the FDA register that we have not verified.

What this manufacturer declares

Class IIa48
Class IIb20

Most frequent device types declared: 10027, 1172, 1179, 1552, 1557.

Among these devices, 68 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 68 declared devices.

Catalogue references include 1172LG30L26, 1172LG30L27, 1179LG12L01, 1179LG20L03, 1179LG2L35E, 1557SH10L16.

European nomenclature codes declared: Q0299, Q02030299.

United States market access

FDA establishment registerSimilar name found — unverified
Matched entryLABORATOIRE UNITHER (FR) · FDA 3010162623
Devices in EUDAMED68
Country of registrationFrance

⚠️ A similar name exists; we do not assert it is the same company — why.

Device-level evidence

Devices with a numeric GTIN68
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryLABORATOIRES THEA

What it holds in Canada

Licences on record6
Currently active0
Class 2 devices6
First licensed2014-01-03

Licence types: Device Family (3), Single Device (3).

Licensed under: THEALOZ DUO, THEALOZ DUO GEL, BLEPHACLEAN, THEAHYABAK, THEALOZ GEL, THEALOZ TOTAL.

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