Axess Vision Technology is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Axess Vision Technology - FDA 510(k) Cleared Devices
Recent clearances: Broncoflex Agile, Broncoflex Vortex, Screeni, Broncoflex Agile
2
Total
2
Cleared
0
Denied
Axess Vision Technology has 2 FDA 510(k) cleared medical devices. Based in Jou?-L?s-Tours, FR.
Last cleared in 2022. Active since 2020. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Axess Vision Technology Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Axess Vision Technology
2 devices