Branemark Integration AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Branemark Integration AB - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Branemark Integration AB has 3 FDA 510(k) cleared medical devices. Based in Gotborg, SE.
Historical record: 3 cleared submissions from 2002 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Branemark Integration AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Branemark Integration AB
3 devices