Naviswiss AG - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Confinis AG as regulatory consultant.
3 devices