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Aecl Medical

CanadaFDA applicant, unverified

Devices
1

What Aecl Medical makes

Aecl Medical manufactures the THERATRON-PHOENIX, a high-energy radiation therapy device designed for targeted cancer treatment using electron beam therapy.

The THERATRON-PHOENIX is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Theratron-Phoenix Ref K863180

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Aecl Medical have in the registry?

The registry currently lists 1 device for Aecl Medical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aecl Medical's devices?

Among its 1 most recently registered device, Aecl Medical has devices listed in FDA 510(k) (1 device).

What risk classes do Aecl Medical's devices fall under?

Among its 1 most recently registered device, the classes recorded for Aecl Medical's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aecl Medical in the registry?

The most recently registered devices listed for Aecl Medical include THERATRON-PHOENIX.

Generated automatically from registry data and not verified by a human reviewer.