Blustone Synergy, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Blustone Synergy, LLC - FDA 510(k) Cleared Devices
Recent clearances: Blustone Synergy Diamond SA Cervical System, Blustone Synergy Interbody Fusion System
2
Total
2
Cleared
0
Denied
Blustone Synergy, LLC has 2 FDA 510(k) cleared medical devices. Based in Pueblo, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Blustone Synergy, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Blustone Synergy, LLC
2 devices