Akili Interactive Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Akili Interactive Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EndeavorOTC, EndeavorRx
3
Total
2
Cleared
1
Denied
Akili Interactive Labs, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boston, US.
Latest FDA clearance: Jun 2024. Active since 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Akili Interactive Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Akili Interactive Labs, Inc.
3 devices