Akros Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Akros Medical - FDA 510(k) Cleared Devices
Recent clearances: Akros Scruture Anchor LisFranc Repair Kit
3
Total
3
Cleared
0
Denied
Akros Medical has 3 FDA 510(k) cleared medical devices. Based in Durham, US.
Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Akros Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Akros Medical
3 devices