Kinos Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kinos Medical - FDA 510(k) Cleared Devices
Recent clearances: Kinos Axiom Total Ankle System
1
Total
1
Cleared
0
Denied
Kinos Medical has 1 FDA 510(k) cleared medical devices. Based in Wayne, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kinos Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Alyssa Schwartz as regulatory consultant.
FDA 510(k) Regulatory Record - Kinos Medical
1 devices