Synoross Dba Osseone is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synoross Dba Osseone - FDA 510(k) Cleared Devices
Recent clearances: OsseOne Dental Implant System, OsseOne Dental Implant System
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.
FDA 510(k) Regulatory Record - Synoross Dba Osseone
2 devices