Dendrite Imaging, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dendrite Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Dendrite Imaging System
1
Total
1
Cleared
0
Denied
Dendrite Imaging, Inc. has 1 FDA 510(k) cleared medical devices. Based in Berkeley, US.
Latest FDA clearance: Nov 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dendrite Imaging, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Decus Biomedical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dendrite Imaging, Inc.
1 devices