Tamabio is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Tamabio - FDA 510(k) Cleared Devices
Recent clearances: PeriBeam® Pericardial Membrane
1
Total
1
Cleared
0
Denied
Tamabio has 1 FDA 510(k) cleared medical devices. Based in Tokyo, JP.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tamabio Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nilo Medical Consulting Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Tamabio
1 devices