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Avantis Medical Systems, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
6

What Avantis Medical Systems, Inc. makes

Avantis Medical Systems, Inc. manufactures auxiliary endoscopy systems, including panoramic and retroscope designs, which assist in visualizing internal anatomical structures during endoscopic procedures. These devices are used to enhance the field of view for surgeons, improving precision during minimally invasive surgeries. The portfolio includes both standard and modified retroscope systems, as well as a reusable version of the panoramic auxiliary endoscopy system.

The company’s devices are classified as Class II under FDA regulations and are recorded in the 510(k) clearance database. The products are intended for use in the United States, where regulatory compliance is required for market authorization.

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

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

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

The registry currently lists 6 devices for Avantis Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Avantis Medical Systems, Inc.'s devices?

Among its 6 most recently registered devices, Avantis Medical Systems, Inc. has devices listed in FDA 510(k) (6 devices).

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

Among its 6 most recently registered devices, the classes recorded for Avantis Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Avantis Medical Systems, Inc. include THIRD EYE PANORAMIC AUXILIARY ENDOSCOPY SYSTEM, THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEM, THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM and MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM.

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