EU → US Device Access

Atesos medical AG

CH-MF-000010304 · Switzerland · Aarau

Atesos medical AG is registered in the European database on medical devices as a manufacturer, with 244 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa135
Class I109

Most frequent device types declared: Pyramid Hip Shell, Trial insert, SORT-P non-sterile, Pyramid Hip Shell Revision, Pyramid Hip Stem.

Among these devices, 110 are declared sterile, 109 implantable, 83 reusable.

Authorised representative in the Union: DE-AR-000006853.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED244
Country of registrationSwitzerland
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

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