Osseofuse International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osseofuse International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HexaPLUS S OneDrill Implant System, Conical Plus Implant System
2
Total
2
Cleared
0
Denied
Osseofuse International, Inc. has 2 FDA 510(k) cleared medical devices. Based in Calabasas, US.
Latest FDA clearance: Oct 2025. Active since 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Osseofuse International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Osseofuse International, Inc.
2 devices