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Etview, Ltd.

Also registered as Etview

IsraelFDA applicant, unverified

Etview, Ltd. is a medical device manufacturer, with 9 devices listed in FDA 510(k) (FDA Class II) as of 13 Nov 2026.

Devices
9

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA 510(k) 9
Device classes
  • FDA Class II 9

What Etview, Ltd. makes

Etview, Ltd. manufactures single-use basic endotracheal tubes, bronchoscopic balloon catheters, and endobronchial tubes, including tracheoscopic ventilation tubes. Their portfolio also includes reusable electrical connection cables and colour image display units for medical imaging, branded under the VivaSight series.

The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance and the FDA’s Unique Device Identifier (UDI) system.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

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

The registry currently lists 9 devices for Etview, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Etview, Ltd.'s devices?

Among its 9 most recently registered devices, Etview, Ltd. has devices listed in FDA 510(k) (9 devices).

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

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

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

The most recently registered devices listed for Etview, Ltd. include VivaSight-SL (TVT) system, DOUBLE LUMEN VIDEO TRACHEOSDOPE (DLVT) SYSTEM, VIVASIGHT-DL SYSTEM and TRACHEOSCOPIC VENTILATION TUBE (TVT).

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