Medical Device Manufacturer · CH , Plan Les Ouates

Medimaps Group SA - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2012

Total

Cleared

Denied

Medimaps Group SA has 3 FDA 510(k) cleared medical devices. Based in Plan Les Ouates, CH.

Latest FDA clearance: Jan 2025. Active since 2012. Primary specialty: Radiology.

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

Medimaps Group 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 - Medimaps Group SA

3 devices

1-3 of 3