Viveve Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viveve Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Viveve System, Viveve 2.0 System, Viveve System, Viveve 2.0 System
3
Total
3
Cleared
0
Denied
Viveve Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Englewood, US.
Last cleared in 2021. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Viveve Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Viveve Medical, Inc.
3 devices