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Carmel Medical Devices

Country not established

Devices
1

What Carmel Medical Devices makes

Carmel Medical Devices manufactures the TROGIDE, a medical device designed for use in transoral robotic surgery procedures.

The TROGIDE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • Trogide Ref K844696

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

Frequently asked questions

How many devices does Carmel Medical Devices have in the registry?

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

Which registries list Carmel Medical Devices's devices?

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

What risk classes do Carmel Medical Devices's devices fall under?

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

What are the newest devices from Carmel Medical Devices in the registry?

The most recently registered devices listed for Carmel Medical Devices include TROGIDE.

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