Medical Device Manufacturer · CH , Lelocle

Medos International S?rl - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2016

Total

Cleared

Denied

Medos International S?rl has 4 FDA 510(k) cleared medical devices. Based in Lelocle, CH.

Last cleared in 2023. Active since 2016. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Medos International S?rl Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Depuy Spine, A Johnson & Johnson Company, Depuy Synthes Spine and Medos International Sàrl.

Medos International S?rl is one of 130 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medos International S?rl

4 devices

1-4 of 4

Data Source

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

Last updated: May 15, 2026