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Cyclotec

Country not established

Devices
1

What Cyclotec makes

Cyclotec manufactures transcutaneous electrical nerve stimulation (TENS) devices, specifically the AMT CTI model, designed for pain management applications. These devices deliver low-voltage electrical currents to the skin to modulate pain signals.

The company’s TENS devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Cyclotec have in the registry?

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

Which registries list Cyclotec's devices?

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

What risk classes do Cyclotec's devices fall under?

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

What are the newest devices from Cyclotec in the registry?

The most recently registered devices listed for Cyclotec include CYCLOTEC AMT CTI TENS DEVICE.

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