Skip to content

Trod Medical SA

FranceFDA 510(k) applicant, unverified

Devices
1

What Trod Medical SA makes

Trod Medical SA manufactures bipolar radiofrequency (RF) probes, specifically designed for surgical applications requiring precise tissue ablation or coagulation. These devices are intended for use in minimally invasive procedures to target and treat abnormal tissue while minimizing damage to surrounding areas.

The company’s bipolar RF probe is classified as a Class II medical device under FDA regulations and is supported by a 510(k) clearance. The device is listed in the FDA’s 510(k) database, adhering to U.S. regulatory requirements for its intended use. The manufacturer 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

  • Encage Bipolar Rf Probe Ref K082954

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Trod Medical SA have in the registry?

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

Which registries list Trod Medical SA's devices?

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

What risk classes do Trod Medical SA's devices fall under?

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

What are the newest devices from Trod Medical SA in the registry?

The most recently registered devices listed for Trod Medical SA include ENCAGE BIPOLAR RF PROBE.

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