Wittenstein Intens GmbH - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Wittenstein Intens GmbH has 2 FDA 510(k) cleared medical devices. Based in Igersheim, DE.
Last cleared in 2021. Active since 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Wittenstein Intens GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wagoner Consulting Llg as regulatory consultant.
FDA 510(k) Regulatory Record - Wittenstein Intens GmbH
2 devices