Inquis Medical - FDA 510(k) Cleared Devices

Inquis Medical has 8 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Latest FDA clearance: Apr 2026. Active since 2023. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Inquis Medical Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mojgan Saadat as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.