Blustone Synergy is one of 18469 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Blustone Synergy - FDA 510(k) Cleared Devices
Recent clearances: Blustone Synergy Silica System
1
Total
1
Cleared
0
Denied
Blustone Synergy has 1 FDA 510(k) cleared medical devices. Based in Pueblo, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Blustone Synergy Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kaedon Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Blustone Synergy
1 devices