Medical Device Manufacturer · SE , Goteborg

Promimic AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Promimic AB has 2 FDA 510(k) cleared medical devices. Based in Goteborg, SE.

Latest FDA clearance: May 2026. Active since 2011. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Promimic AB Filter by specialty or product code using the sidebar.

Promimic AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Promimic AB

2 devices

1-2 of 2