In2bones USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
In2bones USA - FDA 510(k) Cleared Devices
Recent clearances: CoLink NeoFuse MIS Plating System (see attached parts list)
1
Total
1
Cleared
0
Denied
In2bones USA has 1 FDA 510(k) cleared medical devices. Based in Memphis, US.
Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by In2bones USA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - In2bones USA
1 devices