EU → North America Device Access

Frontier Therapeutics Limited

GB-MF-000035429 · United Kingdom · Tredegar

Frontier Therapeutics Limited is registered in the European database on medical devices as a manufacturer, with 702 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa702

Most frequent device types declared: Repose, Toto.

Among these devices, 702 are declared reusable.

Authorised representative in the Union: Frontier Medical Germany GmbH.

Catalogue references include 010325, 079209, 6200100, 6750211, 6801001, 6883022.

European nomenclature codes declared: V080702, V0811, V08030102, V080701.

United States market access

FDA establishment registerRegistered with FDA
Matched entryFRONTIER THERAPEUTICS LIMITED (GB) · FDA 3002798200
Devices in EUDAMED702
Country of registrationUnited Kingdom

Device-level evidence

Devices with a numeric GTIN702
Found in the U.S. device database56
Share8.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: United States only. Frontier Therapeutics Limited is registered in the United States but was not found in the Canadian register.

Other manufacturers in United Kingdom

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