Pure Global

GlassBONE Injectable Putty - Graft, bone, synthetic

Access comprehensive regulatory information for GlassBONE Injectable Putty - Graft, bone, synthetic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Evolution Surgical Pty Ltd, manufactured by Noraker in France. The device registration started on August 19, 2020.

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 III
Class III
GlassBONE Injectable Putty - Graft, bone, synthetic
Australia TGA ARTG Registered Device
Good Name: Evolution Surgical Pty Ltd - GlassBONE Injectable Putty - Graft, bone, synthetic
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Intended Purpose

GlassBONE Injectable Putty is indicated for the filling of bone defects in dental surgery, orthopaedic surgery, spinal surgery and maxillofacial surgery.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
August 19, 2020
Effective Date
August 19, 2020
Manufacturer
Country
France
Address
13 avenue Albert Einstein, Villeurbanne, 69100