Skip to content

Amest Corp.

Country not established

Devices
1

What Amest Corp. makes

Amest Corp. manufactures the MB System, a bioenergy light therapy device designed for therapeutic applications using controlled light exposure.

The MB System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. 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

Frequently asked questions

How many devices does Amest Corp. have in the registry?

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

Which registries list Amest Corp.'s devices?

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

What risk classes do Amest Corp.'s devices fall under?

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

What are the newest devices from Amest Corp. in the registry?

The most recently registered devices listed for Amest Corp. include MB SYSTEM, BIOENERGY LIGHT THERAPY.

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