Bodyport, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bodyport, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Bodyport Cardiac Scale
1
Total
1
Cleared
0
Denied
Bodyport, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bodyport, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Bodyport, Inc.
1 devices