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Client Outlook, Inc.

CanadaFDA applicant, unverified

Devices
3

What Client Outlook, Inc. makes

Client Outlook, Inc. manufactures the eUnity system, a medical device designed for electronic health record (EHR) integration and clinical documentation within healthcare settings. The device supports workflow automation, patient data management, and interoperability between healthcare providers and systems.

The eUnity system is classified as a Class II device under FDA regulations and has been authorised through the 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • eUnity Ref K161515

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • eUnity Ref K172490

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Eunity Ref K111164

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

Frequently asked questions

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

The registry currently lists 3 devices for Client Outlook, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Client Outlook, Inc.'s devices?

Among its 3 most recently registered devices, Client Outlook, Inc. has devices listed in FDA 510(k) (3 devices).

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

Among its 3 most recently registered devices, the classes recorded for Client Outlook, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Client Outlook, Inc. include eUnity.

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