Endophys Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endophys Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: Endophys Blood Pressure Monitor model BPM-30
1
Total
1
Cleared
0
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.
510(k) submissions have been managed by Winegar Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Endophys Technologies, LLC
1 devices