Endocure Technologies, Inc. is one of 16240 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endocure Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EndoCure Model EUR078A
1
Total
1
Cleared
0
Denied
Endocure Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Beltsville, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Endocure Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Endocure Technologies, Inc.
1 devices