Australia TGA ARTG record

Mandible-repositioning/palate-lifting antisnoring orthosis

Australia TGA ARTG Registered Device · The Weringa Group Pty Ltd · Vivos Therapeutics Inc · Class I · Started June 06, 2022

Good Name: The Weringa Group Pty Ltd - Mandible-repositioning/palate-lifting antisnoring orthosis

Device classification

Risk Class: Class I
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: June 06, 2022
Effective Date: June 06, 2022

Sponsor

Name: The Weringa Group Pty Ltd

Manufacturer

Name: Vivos Therapeutics Inc
Country: United States of America
Address: 9137 S Ridgeline Blvd Suite 135, Highland Ranch, CO, 80129

Intended purpose

Intended to reduce nighttime snoring, obstructive sleep apnea and symptoms of sleep disordered breathing.

About this record

Access comprehensive regulatory information for Mandible-repositioning/palate-lifting antisnoring orthosis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by The Weringa Group Pty Ltd, manufactured by Vivos Therapeutics Inc in United States of America. The device registration started on June 06, 2022.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.