Verily Life Sciences, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Verily Life Sciences, LLC - FDA 510(k) Cleared Devices
Recent clearances: Verily Numetric Retinal Camera, Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor, Study Watch with Irregular Pulse Monitor
4
Total
4
Cleared
0
Denied
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. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Verily Life Sciences, LLC
4 devices
Cleared
Dec 09, 2024
Verily Numetric Retinal Camera
Ophthalmic
109d
Cleared
CT
Jul 19, 2022
Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular...
Cardiovascular
280d
Cleared
CT
Jan 17, 2020
Study Watch with Irregular Pulse Monitor
Cardiovascular
135d
Cleared
Jan 17, 2019
Study Watch
Cardiovascular
132d