Bonalive Biomaterials, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Bonalive Biomaterials, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Turku, FI.
Last cleared in 2023. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Bonalive Biomaterials, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Obelix Consulting, LLC as regulatory consultant.
2 devices