Dignitana AB is one of 104 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Dignitana AB - FDA 510(k) Cleared Devices
Recent clearances: DigniCap Scalp Cooling System
2
Total
1
Cleared
1
Denied
Dignitana AB has 1 FDA 510(k) cleared medical devices. Based in Lund, SE.
Historical record: 1 cleared submissions from 2015 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dignitana AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dignitana AB
2 devices