Entac Medical, Inc. - FDA 510(k) Cleared Devices

Entac Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Memphis, US.

Last cleared in 2023. Active since 2021. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by Target Health, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.