Medical Device Manufacturer · US , Potomac , MD

In2bones Sas - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 2014
18
Total
18
Cleared
0
Denied

In2bones Sas has 18 FDA 510(k) cleared orthopedic devices. Based in Potomac, US.

Latest FDA clearance: Apr 2024. Active since 2014.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by In2bones USA as regulatory consultant.

FDA 510(k) Regulatory Record - In2bones Sas
18 devices
1-12 of 18
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