Medical Device Manufacturer · BE , Ghent

Epilog - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

Recent clearances: PreOp

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Epilog Neurology ✕

1 devices

1-1 of 1

Cleared Jan 08, 2018

Neurology · 110d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Jun 10, 2026