Bonalive , Ltd. is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.
Bonalive , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Bonalive Maxillofacial
1
Total
1
Cleared
0
Denied
Bonalive , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Turku, FI.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bonalive , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Obelix Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Bonalive , Ltd.
1 devices