Endolumik, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endolumik, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie)
1
Total
1
Cleared
0
Denied
Endolumik, Inc. has 1 FDA 510(k) cleared medical devices. Based in Morgantown, US.
Last cleared in 2023. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Endolumik, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nilo Medical Consulting Group as regulatory consultant.
FDA 510(k) Regulatory Record - Endolumik, Inc.
1 devices