Endolumik is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endolumik - FDA 510(k) Cleared Devices
Recent clearances: Endolumik Gastric Calibration Tube M Series (EGCT36M)
1
Total
1
Cleared
0
Denied
Endolumik has 1 FDA 510(k) cleared medical devices. Based in Morgantown, US.
Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Endolumik 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
1 devices