Endophys Technologies, LLC - FDA 510(k) Cleared Devices

Endophys Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Dallas, US.

Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Winegar Consulting, Inc. as regulatory consultant.