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Healicoil Knotless Regenesorb Suture Anchor - Fixation anchor, soft-tissue, biodegradable - ARTG 382150

Access comprehensive regulatory information for Healicoil Knotless Regenesorb Suture Anchor - Fixation anchor, soft-tissue, biodegradable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 382150 and sponsored by Smith & Nephew Pty Ltd, manufactured by Smith & Nephew Inc Endoscopy Division in United States of America. The device registration started on January 07, 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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TGA ARTG Official Data
Class III
ARTG 382150
Class III
Healicoil Knotless Regenesorb Suture Anchor - Fixation anchor, soft-tissue, biodegradable
ARTG ID: 382150
Good Name: Smith & Nephew Pty Ltd - Healicoil Knotless Regenesorb Suture Anchor - Fixation anchor, soft-tissue, biodegradable
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Intended Purpose

HEALICOIL Knotless REGENESORB Suture Anchor is intended for use only for the reattachment of soft tissue to bone for the following indications: Shoulder -Biceps tenodesis -Rotator cuff tear repair

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
382150
Start Date
January 07, 2022
Effective Date
January 07, 2022
Manufacturer
Country
United States of America
Address
150 Minuteman Road, ANDOVER, MA, 01810-1031