Synexis, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synexis, LLC - FDA 510(k) Cleared Devices
Recent clearances: Synexis Sphere Rx
1
Total
1
Cleared
0
Denied
Synexis, LLC has 1 FDA 510(k) cleared medical devices. Based in Lenexa, US.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Synexis, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Synexis, LLC
1 devices