Endolumik, Inc. - FDA 510(k) Cleared Devices
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