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Manufacturer profile

Biomet Orthopedics

Manufacturer • United States of America704 devices on the TGA ARTG6 device classesNov 17, 2003 – Jun 27, 2024
VerifiedTGA · Australian Register of Therapeutic Goods
704
Total devices
6
Device classes
2003
Earliest registration
2024
Latest registration
Regulatory footprint
Search Biomet Orthopedics across other regulatory registries
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Recent device registrations
Latest 10 TGA ARTG device registrations
OSS AVL Non-Modular Tibial Baseplate Long - Coated knee tibia prosthesis
Sponsor: Zimmer Biomet Pty Ltd
Class III · Jun 27, 2024
OSS AVL Non-Modular Tibial Baseplate Long - Coated knee tibia prosthesis
ARTG 453821Sponsor: Zimmer Biomet Pty Ltd
Class III · Jun 27, 2024
Suture/needle passer
Sponsor: Zimmer Biomet Pty Ltd
Class I · Feb 28, 2022
Driver, prosthesis
ARTG 384792Sponsor: Zimmer Biomet Pty Ltd
Class I · Feb 28, 2022
Arthroscopic access cannula obturator
ARTG 384809Sponsor: Zimmer Biomet Pty Ltd
Class I · Feb 28, 2022
Suture/needle passer
ARTG 384808Sponsor: Zimmer Biomet Pty Ltd
Class I · Feb 28, 2022
Arthroscopic access cannula obturator
Sponsor: Zimmer Biomet Pty Ltd
Class I · Feb 28, 2022
Driver, prosthesis
Sponsor: Zimmer Biomet Pty Ltd
Class I · Feb 28, 2022
Persona Partial Knee System, Vivacit-E® Highly Crosslinked Polyethylene Partial Articular Surface - Unicondylar knee insert
Sponsor: Zimmer Biomet Pty Ltd
Class III · May 22, 2020
Persona Partial Knee System, Partial Tibia Cemented - Uncoated unicondylar knee tibia prosthesis, metallic
ARTG 336795Sponsor: Zimmer Biomet Pty Ltd
Class III · May 22, 2020
View all 704 devices →
Risk class distribution
Devices by risk class
Class I28340.2% of total
Class IIa588.2% of total
Class IIb497.0% of total
Class III30443.2% of total
Class Is40.6% of total
Class Im60.9% of total
About this profile

Explore comprehensive manufacturer profile for Biomet Orthopedics through Pure Global AI's free Australia TGA ARTG medical device database. This company has manufactured 704 medical devices registered with TGA ARTG across 6 device classes. This manufacturer is based in United States of America. Their registration history spans from Nov 17, 2003 to Jun 27, 2024.

This page provides detailed insights including recent device registrations, risk class distribution (Class III: 304, Class IIa: 58, Class IIb: 49, Class I: 283, Class Im: 6, Class Is: 4), and complete regulatory information from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's medical device registry with 62k records.