Sibel, Inc. - FDA 510(k) Cleared Devices

Sibel, Inc. has 3 FDA 510(k) cleared medical devices. Based in Niles, US.

Last cleared in 2022. Active since 2021. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Sibel, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.