Blue Ocean Global - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Blue Ocean Global has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Blue Ocean Global Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.
1 devices