Australia TGA ARTG record

CUVIS-joint - Robotic surgical system

Australia TGA ARTG Registered Device · LMT Surgical Pty Ltd · Curexo Inc · Class IIa · Started July 15, 2021

Good Name: LMT Surgical Pty Ltd - CUVIS-joint - Robotic surgical system

Device classification

Risk Class: Class IIa
Product Type: Medical device system
ARTG Category: General

Registration information

Start Date: July 15, 2021
Effective Date: July 15, 2021

Sponsor

Name: LMT Surgical Pty Ltd

Manufacturer

Name: Curexo Inc
Country: South Korea
Address: 3rd/4th Floor 577 Gangnam-daero, Seocho-Gu, Seoul, 06530

Intended purpose

intended for use as a stereotaxic device for knee arthroplasty. It is to assist a surgeon in planning of pre-operation using medical diagnostic images obtained from patient and to provide orientation and reference information during intraoperative procedures. The surgical tools, under the supervision of the surgeon, perform the preoperative surgical plan.

About this record

Access comprehensive regulatory information for CUVIS-joint - Robotic surgical system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by LMT Surgical Pty Ltd, manufactured by Curexo Inc in South Korea. The device registration started on July 15, 2021.

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.