Ndd Medizintechnik AG is one of 129 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Ndd Medizintechnik AG - FDA 510(k) Cleared Devices
Recent clearances: EasyOne Sky Spirometer, EasyOne Filter, EasyOne Pro Respiratory Analysis System
4
Total
4
Cleared
0
Denied
Ndd Medizintechnik AG has 4 FDA 510(k) cleared medical devices. Based in Zurich, CH.
Last cleared in 2023. Active since 2017. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Ndd Medizintechnik AG Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Ndd Medical Technologies, Inc. and Ndd Medical Technologies.
FDA 510(k) Regulatory Record - Ndd Medizintechnik AG
4 devices