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MICRORAPTOR™ REGENESORB Suture Anchor - Fixation anchor, soft-tissue, biodegradable

Access comprehensive regulatory information for MICRORAPTOR™ 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 sponsored by Smith & Nephew Pty Ltd, manufactured by Smith & Nephew Inc Endoscopy Division in United States of America. The device registration started on November 17, 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
MICRORAPTOR™ REGENESORB Suture Anchor - Fixation anchor, soft-tissue, biodegradable
Australia TGA ARTG Registered Device
Good Name: Smith & Nephew Pty Ltd - MICRORAPTOR™ REGENESORB Suture Anchor - Fixation anchor, soft-tissue, biodegradable
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Intended Purpose

The Smith & Nephew MICRORAPTOR REGENESORB Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications: Hip Acetabular labrum repair/reconstruction Shoulder • Capsular stabilization –– Bankart repair –– Anterior shoulder instability –– SLAP lesion repairs –– Capsular shift or capsulolabral reconstructions • Biceps tenodesis

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
November 17, 2020
Effective Date
November 17, 2020
Manufacturer
Country
United States of America
Address
150 Minuteman Road, ANDOVER, MA, 01810-1031