Synoross Dba Osseone - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Synoross Dba Osseone has 2 FDA 510(k) cleared medical devices. Based in Glendale, US.
Latest FDA clearance: May 2025. Active since 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Synoross Dba Osseone Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
2 devices