Suzon Lommel

Senior Vice President of Regulatory & Quality Affairs

Suzon Lommel, Viveve’s Senior Vice President of Regulatory and Quality Affairs, joined the Company in 2016 with more than 30 years of experience in the medical device industry developing regulatory and quality systems. Prior to joining Viveve, she was Global Vice President of Regulatory and Quality Affairs at Ulthera, Inc. which was acquired by Merz Aesthetics in July 2014. Her prior experience includes executive and senior management roles at Breathe Technologies, Inc., FoxHollow Technologies, Inc., Advanced Stent Technology, and Boston Scientific. Ms. Lommel has extensive experience with the U.S. Food and Drug Administration and international regulatory agencies. She has authored numerous 510k, IDE, PMA, and international submissions.

Ms. Lommel holds a degree in Physics from Moorpark College.

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Product Indications

Viveve System
The Viveve System is indicated for general surgery for electrocoagulation and hemostasis in the United States.
Viveve Solutions
The Viveve System is indicated for general surgery for electrocoagulation and hemostasis in the United States. The InControl Products (InToneMV) is indicated for the treatment of all forms of urinary incontinence in the United States and Canada.