Osseofuse International, Inc. - FDA 510(k) Cleared Devices
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.
2 devices