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Cosmetic phototherapy system, home-use - ARTG 464865

Access comprehensive regulatory information for Cosmetic phototherapy system, home-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 464865 and sponsored by Fringe Australia Pty Ltd, manufactured by Shenzhen Kaiyan Medical Equipment Co Ltd in China. The device registration started on October 18, 2024.

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.

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TGA ARTG Official Data
Class IIa
ARTG 464865
Class IIa
Cosmetic phototherapy system, home-use
ARTG ID: 464865
Good Name: Fringe Australia Pty Ltd - Cosmetic phototherapy system, home-use
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Intended Purpose

The Fringe light therapy face mask is an over the counter device that is intended for the use in the treatment of full-face wrinkles and treat mild to moderate acne vulgaris of the face.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
464865
Start Date
October 18, 2024
Effective Date
October 18, 2024
Manufacturer
Country
China
Address
Building #3 and Building #5 40th of Fuxin Street Huaide Community Fuyong Town, Baoan District Shenzhen, Guangdong, 518103