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Vista Medical Technologies, Inc.

United StatesFDA applicant, unverified

Devices
9

What Vista Medical Technologies, Inc. makes

Vista Medical Technologies, Inc. manufactures surgical visualization and imaging systems, including stereoscopic viewing devices, head-mounted displays, and illumination systems for operating rooms. Their portfolio includes single-chip video cameras, intraoperative software solutions like the ORPC with Infomatrix, and specialized telescopes for minimally invasive procedures. Additional offerings include voice-activated visualization systems and wide-angle telescopes designed for autoclaving.

The company’s devices are classified under Class II by the FDA and are listed in the 510(k) registry. These products are intended for use in surgical environments and are regulated under U.S. medical device laws. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

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Frequently asked questions

How many devices does Vista Medical Technologies, Inc. have in the registry?

The registry currently lists 9 devices for Vista Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vista Medical Technologies, Inc.'s devices?

Among its 9 most recently registered devices, Vista Medical Technologies, Inc. has devices listed in FDA 510(k) (9 devices).

What risk classes do Vista Medical Technologies, Inc.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Vista Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Vista Medical Technologies, Inc. in the registry?

The most recently registered devices listed for Vista Medical Technologies, Inc. include VISTA ORPC WITH INFOMATIX INTRAOP SOFTWARE, MODIFICATION TO VISTA STEREOSCOPE SYSTEM, VISTA SINGLE CHIP VIDEO CAMERA and HEAD MOUNTED DISPLAY.

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