Vivorte, Inc. is one of 18464 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vivorte, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vivorte Trabexus EB, Vivorte Trabexus, VIVORTE BVF
4
Total
4
Cleared
0
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.
510(k) submissions have been managed by Peoples & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Vivorte, Inc.
4 devices