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Sanolla, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Sanolla, Ltd. makes

Sanolla, Ltd. manufactures the VoqX Electronic Stethoscope, a digital stethoscope designed for enhanced auscultation in clinical settings.

The VoqX Electronic Stethoscope is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • VoqX Electronic Stethoscope Ref K212709

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

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

The registry currently lists 1 device for Sanolla, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sanolla, Ltd.'s devices?

Among its 1 most recently registered device, Sanolla, Ltd. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Sanolla, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Sanolla, Ltd. include VoqX Electronic Stethoscope.

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