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Sensormed

Country not established

Devices
2

What Sensormed makes

Sensormed manufactures CABLECAP devices, including models WLF, STZ, and ACM, which are designed for medical monitoring applications involving cable connections and signal transmission.

The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. Sensormed is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Cablecap Model: Wlf, Stz, Acm Ref K101496

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cablecap Ref K113330

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

Frequently asked questions

How many devices does Sensormed have in the registry?

The registry currently lists 2 devices for Sensormed. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sensormed's devices?

Among its 2 most recently registered devices, Sensormed has devices listed in FDA 510(k) (2 devices).

What risk classes do Sensormed's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Sensormed's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Sensormed in the registry?

The most recently registered devices listed for Sensormed include CABLECAP MODEL: WLF, STZ, ACM and CABLECAP.

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