Visionsense, Ltd. - FDA 510(k) Cleared Devices

Visionsense, Ltd. has 13 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2022. Active since 2008. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Visionsense, Ltd. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Licensale, Inc. and Hogan Lovells US LLP.