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Dental implant analog - ARTG 471267

Access comprehensive regulatory information for Dental implant analog in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 471267 and sponsored by DIO Australia Pty Ltd, manufactured by DIO Corporation in South Korea. The device registration started on December 02, 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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Class I
ARTG 471267
Class I
Dental implant analog
ARTG ID: 471267
Good Name: DIO Australia Pty Ltd - Dental implant analog
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Intended Purpose

A device intended to be used as a copy of a dental implant, for a dental laboratory working model, to duplicate the location and restorative platform orientation of the final dental implant; it is not intended for intraoral use. It is a rod-like device made of metal [e.g., titanium (Ti)]. This is a single-use device.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
471267
Start Date
December 02, 2024
Effective Date
December 02, 2024
Manufacturer
Country
South Korea
Address
66 Centum seo-ro Haeundae-gu, Busan, 48058