Medical Device Manufacturer · US , Calabasas , CA

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

2 submissions · 2 cleared · Since 2019

Total

Cleared

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.

FDA 510(k) cleared devices by Osseofuse International, Inc.

2 devices

1-2 of 2