Medical Device Manufacturer · CH , Villette (Lavaux)

Neo Medical SA - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2017

Total

Cleared

Denied

Neo Medical SA has 6 FDA 510(k) cleared medical devices. Based in Villette (Lavaux), CH.

Latest FDA clearance: Dec 2024. Active since 2017. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Neo Medical SA Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Meditec Consulting GmbH, Confinis USA and Confinis Corporation.

Neo Medical SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neo Medical SA

6 devices

1-6 of 6

Data Source

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

Last updated: May 10, 2026