Medical Device Manufacturer · CH , Renens

Lumendo AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023

Recent clearances: Fibercure, Endofill

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Lumendo AG Dental ✕

2 devices

1-2 of 2

Cleared Nov 02, 2023

Cleared Jul 10, 2023

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 16, 2026