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Civnet Communication, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Civnet Communication, Ltd. makes

Civnet Communication, Ltd. manufactures the CIV-OB (PLUS), a medical device designed for obstetric communication and monitoring in clinical settings.

The CIV-OB (PLUS) is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Civ-Ob (Plus) Ref K103172

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

Frequently asked questions

How many devices does Civnet Communication, Ltd. have in the registry?

The registry currently lists 1 device for Civnet Communication, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Civnet Communication, Ltd.'s devices?

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

What risk classes do Civnet Communication, Ltd.'s devices fall under?

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

What are the newest devices from Civnet Communication, Ltd. in the registry?

The most recently registered devices listed for Civnet Communication, Ltd. include CIV-OB (PLUS).

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