VivAer® Patient Testimonial: LeAnna, Surgical Technologist

LeAnna a Certified Surgical Technologist works with ENTs and was diagnosed with nasal airway obstruction (NAO) due to nasal valve collapse. Like millions of NAO sufferers, LeAnna experienced issues with nasal breathing, running out of breath, quality of sleep, and mouth breathing. At her doctor's recommendation she decided to seek treatment with VivAer. Watch how LeAnna now has more energy, sleeps better, and keeps up with her young family after being treated with VivAer.
A blocked-up nose shouldn't shut down your life. Many of the millions of patients suffering from nasal airway obstruction (NAO) are frustrated by their quality of life and would welcome a way to find proven, long-lasting relief from their condition. VivAer is an office-friendly, incisionless, non-invasive procedure that offers patients freedom from NAO. VivAer is a non-invasive technology that uses patented, temperature-controlled radiofrequency energy and is clinically demonstrated to provide long-term relief from nasal obstruction.
VivAer features a thin, wand-like stylus that attaches to a console. The stylus is inserted via the nostril to gently remodel the nasal tissue and improve airflow. It is a single solution that is used to treat the lateral nasal wall; it can also treat the turbinates and septal swell bodies that contribute to NAO. VivAer does not involve any cutting, freezing, or removal of nasal tissue or bone. Treatment with VivAer may be performed during a routine office visit with local anesthesia. Patients typically experience little discomfort with minimal downtime, and are often able to return to normal activities immediately following treatment.*
IMPORTANT PATIENT INFORMATION: Please consult with your medical provider regarding specific questions and important information related to VivAer® indications, contraindications, and potential side effects. Rx only.
Specific indications, contraindications, warnings, precautions and safety information exist for these products. Aerin Medical relies on the physician to determine, assess and communicate to each patient all foreseeable risks of the procedure. A physician must always refer to the package insert, product label and/or instructions for use before using any of Aerin Medical’s products.
Prior to use, refer to the “Instructions for Use” for complete and specific indications, contraindications, all warnings and precautions. The VivAer Stylus received CE Mark in 2016 and FDA 510(k) clearance in December 2017. Aerin Medical products and associated components are not available in all countries or regions. Please consult with your Aerin Medical® representative for details regarding product availability.
*Individual results may vary.
Aerin Medical Inc., Aerin, the Aerin Medical Logo and VivAer are registered trademarks of Aerin Medical, Inc. ©2024 Aerin Medical, Inc. All rights reserved. MKT2209.A