Hi-D Imaging AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Hi-D Imaging AG - FDA 510(k) Cleared Devices
Recent clearances: Hi-D Imaging 4TAVR
2
Total
2
Cleared
0
Denied
Hi-D Imaging AG has 2 FDA 510(k) cleared medical devices. Based in Winterthur, CH.
Latest FDA clearance: Jul 2026. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Hi-D Imaging AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Veranex, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hi-D Imaging AG
2 devices