Sonu vs NeoSurround US

SONU provides personalized, drug free, acoustic resonance therapy to treat nasal congestion symptoms caused by allergic and non-allergic rhinitis. SONU is backed by FDA authorization, extensive clinical trials, and enhanced by AI. SONU works with iPhone X or later models and uses Bluetooth to connect with your iPhone. To get started simply download the app and follow the on-screen instructions to get to your 15 minute treatment session. You can choose to relax with the gentle micro vibrations or go about your daily activities. The SONU app takes a scan of your face using the front facing camera and personalizes the acoustic therapy based on your facial anatomy and other proprietary factors. The acoustic resonance is delivered via medical grade bone conduction transducers in the SONU band (a lightweight, wearable headband purchased separately).  SONU is proven to be safe and effective and also has a history of your treatment sessions in the app so you can track your usage over time.  Medical Disclaimer: This app does not replace or provide medical advice and diagnosis. Always seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition. Regulatory Jurisdiction: The SONU band is authorized for use by regulatory authorities only in the USA (FDA) and Singapore (HSA). Any feedback? Contact us at https://soundhealth.life/contact/ Additional information including the privacy policy, biometric notice and terms of use can be found at https://soundhealth.life

NeoSurround is an advanced wellness device designed to integrate seamlessly into your daily routine. Whether you’re looking to support focus, promote relaxation, or create a more restful environment, NeoSurround helps enhance your overall well-being. Important Notice: NeoSurround is intended for relaxation and general wellness purposes only. It is not intended to diagnose, treat, cure, or prevent any disease. Always consult a qualified healthcare professional before making medical decisions or if you have any medical condition, are pregnant, have an implanted medical device, or are under medical supervision. JURISDICTION STATEMENT: In the United States, the connected device is registered and listed with the U.S. Food and Drug Administration (FDA) as a Class I medical device under 21 CFR 890.5660 (Product Code: ISA). In all other jurisdictions, the device is marketed and distributed exclusively as a general wellness product and is not classified, regulated, or promoted as a medical device.