Syneris is one of 500 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Syneris - FDA 510(k) Cleared Devices
Recent clearances: Syneris PACS v.1.0.1.0
1
Total
1
Cleared
0
Denied
Syneris has 1 FDA 510(k) cleared medical devices. Based in Concord, CA.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Syneris Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syneris
1 devices