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Cybercare, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
2

What Cybercare, Inc. makes

Cybercare, Inc. manufactures electronic health care (EHC) desktop patient stations and core provider stations, designed for clinical and administrative use in healthcare settings. These devices support patient monitoring, documentation, and workflow integration within medical environments.

The company’s products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. These devices are based in the United States and comply with applicable U.S. regulatory requirements.

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

Catalogue2

Newest first, rows 1-2 of 2

Frequently asked questions

How many devices does Cybercare, Inc. have in the registry?

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

Which registries list Cybercare, Inc.'s devices?

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

What risk classes do Cybercare, Inc.'s devices fall under?

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

What are the newest devices from Cybercare, Inc. in the registry?

The most recently registered devices listed for Cybercare, Inc. include EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION and EHC500 DESKTOP PATIENT STATION, MODEL EHC500.

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