Envisiontec GmbH - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Envisiontec GmbH has 5 FDA 510(k) cleared medical devices. Based in Gladbeck, DE.
Last cleared in 2022. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Envisiontec GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.
5 devices