EU → North America Device Access

Estetic Ceram AG

LI-MF-000001476 · Liechtenstein · Triesen

Estetic Ceram AG is registered in the European database on medical devices as a manufacturer, with 708 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa708

Among these devices, 708 are declared implantable.

Devices declared under this manufacturer

Showing 12 of 708 declared devices.

Catalogue references include 110803, 140220, 141620, 143615, 145120, 77623398.

European nomenclature codes declared: Q010199.

United States market access

FDA establishment registerRegistered with FDA
Matched entryESTETIC CERAM AG (LI) · FDA 3009081830
Devices in EUDAMED708
Country of registrationLiechtenstein

Device-level evidence

Devices with a numeric GTIN708
Found in the U.S. device database85
Share12.0 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryESTETIC CERAM AG

What it holds in Canada

Licences on record5
Currently active0
Class 3 devices5
First licensed2017-04-03

Licence types: Device Family (3), System (2).

Licensed under: ESTETIC CERAM ZIRKON, ESTETIC CERAM HS10PC, ESTETIC CERAM STAINS LFU, ESTETIC CERAM CLASSIC920, ESTETIC CERAM STRUCTURE.

North American profile: Both markets. Estetic Ceram AG is registered in both the United States and Canada.

Other manufacturers in Liechtenstein

All Liechtenstein manufacturers →