Verily Life Sciences, LLC - FDA 510(k) Cleared Devices

Verily Life Sciences, LLC has 4 FDA 510(k) cleared medical devices. Based in South San Francisco, US.

Latest FDA clearance: Dec 2024. Active since 2019. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Verily Life Sciences, LLC 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.