Fitbit, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fitbit, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Fitbit Irregular Rhythm Notifications, Fitbit ECG App
3
Total
3
Cleared
0
Denied
Fitbit, Inc. has 3 FDA 510(k) cleared medical devices. Based in Fairfax, US.
Last cleared in 2022. Active since 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Fitbit, Inc. Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Fitbit, Inc.
3 devices