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Planar Systems, Inc.

United StatesFDA applicant, unverified

Devices
4

What Planar Systems, Inc. makes

Planar Systems, Inc. manufactures digital flat-panel display systems designed for medical imaging, including color and grayscale models such as the DOME CX series and PLANAR DOME EX series. These systems are intended for use in radiology and diagnostic imaging environments, providing high-resolution visual output for X-ray, CT, and other imaging modalities. The company also produces dome-enclosed display systems like the Model DOME E2C, which integrate screens with protective housings for controlled viewing conditions.

The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are intended for use within the United States, adhering to FDA compliance standards for digital imaging displays. The manufacturer is based in the US.

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

Catalogue4

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Frequently asked questions

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

The registry currently lists 4 devices for Planar Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Planar Systems, Inc.'s devices?

Among its 4 most recently registered devices, Planar Systems, Inc. has devices listed in FDA 510(k) (4 devices).

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

Among its 4 most recently registered devices, the classes recorded for Planar Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Planar Systems, Inc. include PLANAR DOME EX LINE MODEL DOME E2C, DOME CX DIGITAL FLAT-PANEL DISPLAY SYSTEM MODEL, C3 COLOR AND C3 GRAY, PLANAR DOME EX SERIES DIGITAL FLAT-PANEL DISPLAY SYSTEM, MODEL E4C COLOR and DOME CX DIGITAL FLAT-PANEL DISPLAY SYSTEM, MODELS C2 AND C5I.

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