Venus Concept Secures FDA 510(k) Clearance for Venus NOVA Platform

Reuters11-10

Venus Concept Secures FDA 510(k) Clearance for Venus NOVA Platform

Venus Concept Inc. has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Venus NOVA™ platform, a next-generation, multi-application device for non-invasive body, face, and skin treatments. This marks the first product clearance under the company's new R&D strategy. The Venus NOVA is set to launch commercially in the U.S. in December 2025, with global rollouts planned for 2026 and beyond. No other organizations were mentioned as recipients of this regulatory approval.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Venus Concept Inc. published the original content used to generate this news brief on November 10, 2025, and is solely responsible for the information contained therein.

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