Cyncronus, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Cyncronus, LLC has 1 FDA 510(k) cleared medical devices. Based in Bothel, US.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cyncronus, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cyncronus, LLC
1 devices