Valeris Medical is one of 13027 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Valeris Medical - FDA 510(k) Cleared Devices
Recent clearances: Apollo Suture Anchor System, BoneCam Suture Anchors, Apollo Suture Anchor System and Titan Screws
3
Total
3
Cleared
0
Denied
Valeris Medical has 3 FDA 510(k) cleared medical devices. Based in Marietta, US.
Historical record: 3 cleared submissions from 2014 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Valeris Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wagoner Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Valeris Medical
3 devices