Bonalive Biomaterials, Ltd. is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.
Bonalive Biomaterials, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Bonalive Orthopedics granules, BonAlive Granules
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.
Regulatory submissions have been managed by Obelix Biotech Solutions and Obelix Consulting, LLC.
FDA 510(k) Regulatory Record - Bonalive Biomaterials, Ltd.
2 devices