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Corventis, Inc.

United StatesFDA applicant, unverified

Devices
7

What Corventis, Inc. makes

Corventis, Inc. manufactures cardiac monitoring systems, including the Nuvant Cardiac Event Monitoring System and the Nuvant Mobile Cardiac Telemetry (MCT) System. These devices enable continuous or intermittent remote monitoring of cardiac activity for patients, with some models also supporting mobile patient management features. The Avivo Mobile Patient Management System integrates with these telemetry solutions to provide real-time data transmission and patient tracking.

The company’s portfolio is regulated under Class II medical devices in the U.S. and is listed in the FDA’s 510(k) clearance registry. These devices are intended for use in cardiac monitoring and telemetry applications. Corventis, Inc. is based in the United States.

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

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Corventis, Inc. have in the registry?

The registry currently lists 7 devices for Corventis, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Corventis, Inc.'s devices?

Among its 7 most recently registered devices, Corventis, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Corventis, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Corventis, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Corventis, Inc. in the registry?

The most recently registered devices listed for Corventis, Inc. include NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM, NUVANT MCT SYSTEM, NUVANT, MOBILE CARDIAC TELEMETRY and AVIVO MOBILE PATIENT MANAGEMENT.

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