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Gi View, Ltd.

Country not established

Gi View, Ltd. is a medical device manufacturer, with 10 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.

Devices
10

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 6
  • FDA 510(k) 4

A device listed in two registries counts in both.

Device classes
  • FDA Class II 10
Sites and related companies

What Gi View, Ltd. makes

Gi View, Ltd. makes flexible video colonoscopes, including the Aer-O-Scope Colonoscope System, which is a single-use device. The company's products also include related accessories such as the Aer-O-Scope Daily Tube Convenience Kit and the Aer-O-Scope Water Bottle.

The company's portfolio is regulated as Class II devices and is listed in the FDA's 510(k) and UDI registries.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Sites1

Frequently asked questions

How many devices does Gi View, Ltd. have in the registry?

The registry currently lists 10 devices for Gi View, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Gi View, Ltd.'s devices?

Among its 10 most recently registered devices, Gi View, Ltd. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Gi View, Ltd.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Gi View, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Gi View, Ltd. in the registry?

The most recently registered devices listed for Gi View, Ltd. include SOLO SCOPE Video Controller 1, SOLO SCOPE Disposable Colonoscope 1, Aer-O-Scope Disposable Colonoscope and Solo Scope Colonoscope System.

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