Medical Device Manufacturer · US , Morgantown , WV

Endolumik - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
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
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