Medical Device Manufacturer · US , Dallas , TX

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

1 submissions · 1 cleared · Since 2023

Total

Cleared

Denied

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.

FDA 510(k) cleared devices by Endophys Technologies, LLC

1 devices

1-1 of 1