Naviswiss AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Naviswiss AG - FDA 510(k) Cleared Devices
Recent clearances: Naviswiss Knee, NAVIPLAN - CT Planning Software for Total Hip Replacement, Naviswiss Hip Navigation System
3
Total
3
Cleared
0
Denied
Naviswiss AG has 3 FDA 510(k) cleared medical devices. Based in Brugg, CH.
Last cleared in 2023. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Naviswiss AG Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Confinis AG and Confinis.
FDA 510(k) Regulatory Record - Naviswiss AG
3 devices