Entac Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Entac Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PrevisEA Device, PrevisEA Device
2
Total
2
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Entac Medical, Inc.
2 devices