Aventix Medical, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Aventix Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Laguna Hills, US.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Aventix Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Albatross Regulatory Consulting as regulatory consultant.
1 devices