Medical Device Manufacturer · US , Fort Wayne , IN

Vivorte, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2013

Total

Cleared

Denied

Vivorte, Inc. has 4 FDA 510(k) cleared medical devices. Based in Fort Wayne, US.

Historical record: 4 cleared submissions from 2013 to 2015. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Vivorte, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vivorte, Inc.

4 devices

1-4 of 4