Promimic AB is one of 142 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Promimic AB - FDA 510(k) Cleared Devices
Recent clearances: Promimic ZrP Surface Dental Implant, PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 8.5 MM MODEL 03-1001, PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 10 MM MODEL 03-1
2
Total
2
Cleared
0
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.
FDA 510(k) Regulatory Record - Promimic AB
2 devices