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Dataview Imaging Intl., Inc.

United StatesFDA applicant, unverified

Devices
2

What Dataview Imaging Intl., Inc. makes

Dataview Imaging Intl., Inc. makes image transport devices, specifically the IMAGE TRANSPORT SERIES III and IMAGE TRANSPORT SERIES II.

These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Image Transport Series Iii Ref K925964

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Image Transport Series Ii Ref K925963

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

Frequently asked questions

How many devices does Dataview Imaging Intl., Inc. have in the registry?

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

Which registries list Dataview Imaging Intl., Inc.'s devices?

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

What risk classes do Dataview Imaging Intl., Inc.'s devices fall under?

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

What are the newest devices from Dataview Imaging Intl., Inc. in the registry?

The most recently registered devices listed for Dataview Imaging Intl., Inc. include IMAGE TRANSPORT SERIES III and IMAGE TRANSPORT SERIES II.

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