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Resin-composite dental cement

Australia TGA ARTG Registered Device · GLEN DENTAL PTY LTD · Vericom Co Ltd · Class IIa · Started April 22, 2022

Good Name: GLEN DENTAL PTY LTD - Resin-composite dental cement

Device classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration information
Start Date
April 22, 2022
Effective Date
April 22, 2022
Sponsor
Manufacturer
Country
South Korea
Address
48 Toegyegongdan 1-gil , Chuncheon-si, Gangwon-do, 200-944
Intended purpose

Denfil is indicated for restorations of class I, II, V of posterior teeth, class III, IV, V of anterior teeth and cervical cavities (wedge shaped defect) involving root surfaces Denfil Flow is indicated for restorations of class V (cervical cavities, root erosion, wedge shaped defects), Class III and IV anterior restorations, small posterior restorations, extended fissures sealing in molars and premolars, repair of composite, ceramic veneers, and blocking out of undercuts.

About this record

Access comprehensive regulatory information for Resin-composite dental cement in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by GLEN DENTAL PTY LTD, manufactured by Vericom Co Ltd in South Korea. The device registration started on April 22, 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.

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