Bios S.R.L. - FDA 510(k) Cleared Devices

Bios S.R.L. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Silver Spring, US.

Latest FDA clearance: Dec 2024. Active since 2005.

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.