Venus Concept, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Venus Concept, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Venus Nova (FP-2001), Venus Versa PRO System
2
Total
2
Cleared
0
Denied
Venus Concept, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Nov 2025. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Venus Concept, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Venus Concept USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Venus Concept, Inc.
2 devices