Intervention Tech, Inc. ; dba Corvention is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intervention Tech, Inc. ; dba Corvention - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Intervention Tech, Inc. ; dba Corvention has 1 FDA 510(k) cleared medical devices. Based in Flagstaff, US.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intervention Tech, Inc. ; dba Corvention Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ikigai Medical Development as regulatory consultant.
Intervention Tech, Inc. ; dba Corvention — FDA 510(k) Products and Clearance History
1 devices