Artventive Medical Group, Inc. is one of 18444 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Artventive Medical Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOS, Endoluminal Occlusion System-EOS, ENDOLUMINAL OCCLUSION SYSTEM (EOS)
3
Total
3
Cleared
0
Denied
Artventive Medical Group, Inc. has 3 FDA 510(k) cleared medical devices. Based in Woodinville, US.
Last cleared in 2022. Active since 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Artventive Medical Group, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Northwest Clinical Research Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Artventive Medical Group, Inc.
3 devices