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Sign in to claim this brandGLOBAL MANUFACTURING TECHNOLOGY PTY LIMITED
US
Last updated May 24, 2026
What GLOBAL MANUFACTURING TECHNOLOGY PTY LIMITED makes
The company manufactures orthopaedic devices for hip replacement surgery, including one-piece press-fit hip femur prostheses, orthopaedic broaches, and femoral stem prosthesis trials. It also produces reusable surgical tools such as aiming/guiding blocks, implant inserters/extractors, and instrument connectors designed for orthopaedic procedures.
All listed devices fall under Class II regulatory classification and are registered in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Global Manufacturing Technology Pty Limited manufacture?
Global Manufacturing Technology Pty Limited specializes in orthopaedic devices primarily used in hip replacement surgery. Their product line includes one-piece press-fit hip femur prostheses, orthopaedic broaches, femoral stem prosthesis trials, and reusable surgical tools such as aiming/guiding blocks, implant inserters/extractors, and instrument connectors. These devices are designed to assist surgeons in precise orthopaedic procedures.
Where is Global Manufacturing Technology Pty Limited based?
The company is based in the United States. This location is relevant for regulatory compliance, manufacturing operations, and distribution of their orthopaedic devices.
Which regulatory registries list Global Manufacturing Technology Pty Limited’s devices?
Global Manufacturing Technology Pty Limited’s devices are registered in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to identify and track specific devices.
How are Global Manufacturing Technology Pty Limited’s devices classified under medical device regulations?
All of Global Manufacturing Technology Pty Limited’s listed devices fall under Class II regulatory classification. This classification typically applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as orthopaedic implants and surgical tools.
Are Global Manufacturing Technology Pty Limited’s devices part of a specific product line or brand?
The company’s devices are marketed under the Paragon brand. This branding likely reflects a focus on precision, durability, and compatibility for orthopaedic procedures, though the specific design and features of each device would depend on its intended use within hip replacement surgery.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- globalortho.com.au
- —
- —
- [email protected]
- Phone
- +6128870100
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 752039982
Catalogue (166)
Page 1 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Paragon | GM08001-206-04 | FDA UDI | Class II | Active |
| Paragon | GM08001-208-04 | FDA UDI | Class II | Active |
| Paragon | GM08001-321-07 | FDA UDI | Class II | Active |
| Paragon | GM08001-208-08 | FDA UDI | Class II | Active |
| GRU Femur | GRU-RL/LM-0F-C | FDA UDI | Class II | Unknown |
| Paragon | GM08001-210-09 | FDA UDI | Class II | Active |
| Paragon | GM08001-211-11 | FDA UDI | Class II | Active |
| GRU Femur | GRU-RM/LL-4F-C | FDA UDI | Class II | Unknown |
| Paragon | GM08001-210-06 | FDA UDI | Class II | Active |
| GRU Tibia | GRU-5T-9.5-P-R | FDA UDI | Class II | Unknown |
| GRU Tibia | GRU-4T-6.5-P-R | FDA UDI | Class II | Unknown |
| Paragon | GM08001-211-09 | FDA UDI | Class II | Active |
| Paragon | GM08001-210-08 | FDA UDI | Class II | Active |
| Paragon | GM08001-211-04 | FDA UDI | Class II | Active |
| RBK Patello Femoral | GO-1003-28-00 | FDA UDI | Class II | Unknown |
| GRU Femur | GRU-RM/LL-3F-C | FDA UDI | Class II | Unknown |
| Paragon | GM08001-207-01 | FDA UDI | Class II | Active |
| Paragon | GM08001-349-03 | FDA UDI | Class II | Active |
| Paragon | GM08001-323-00 | FDA UDI | Class II | Active |
| Paragon | GM08001-211-12 | FDA UDI | Class II | Active |
| Paragon | GM08001-209-08 | FDA UDI | Class II | Active |
| Paragon | GM08001-301-00 | FDA UDI | Class II | Active |
| Paragon | GM08001-210-03 | FDA UDI | Class II | Active |
| GRU Tibia | GRU-6T-9.5-P-R | FDA UDI | Class II | Unknown |
| Paragon | GM08001-207-05 | FDA UDI | Class II | Active |
| RBK Patello Femoral | GO-1003-32-00 | FDA UDI | Class II | Unknown |
| Paragon | GM08001-322-07 | FDA UDI | Class II | Active |
| GRU Tibia | GRU-0T-9.5-P-R | FDA UDI | Class II | Unknown |
| Paragon | GM08001-209-10 | FDA UDI | Class II | Active |
| Paragon | GM08001-206-12 | FDA UDI | Class II | Active |
| Paragon | GM08001-207-03 | FDA UDI | Class II | Active |
| Paragon | GM08001-321-03 | FDA UDI | Class II | Active |
| Paragon | GM08001-208-10 | FDA UDI | Class II | Active |
| Paragon | GM08001-206-02 | FDA UDI | Class II | Active |
| RBK Patello Femoral | GO-6000-0PFL-01 | FDA UDI | Class II | Unknown |
| Paragon | GM08001-349-10 | FDA UDI | Class II | Active |
| Paragon | GM08001-210-12 | FDA UDI | Class II | Active |
| GRU Tibia | GRU-3T-9.5-P-R | FDA UDI | Class II | Unknown |
| GRU Tibia | GRU-0T-6.5-P-R | FDA UDI | Class II | Unknown |
| Paragon | GM08001-206-01 | FDA UDI | Class II | Active |
| GRU Tibia | GRU-1T-7.5-P-R | FDA UDI | Class II | Unknown |
| Paragon | GM08001-211-02 | FDA UDI | Class II | Active |
| Paragon | GM08001-322-06 | FDA UDI | Class II | Active |
| Paragon | GM08001-211-07 | FDA UDI | Class II | Active |
| Paragon | GM08001-209-03 | FDA UDI | Class II | Active |
| Paragon | GM08001-321-05 | FDA UDI | Class II | Active |
| Paragon | GM08001-206-07 | FDA UDI | Class II | Active |
| Paragon | GM08001-209-09 | FDA UDI | Class II | Active |
| GRU Tibia | GRU-5T-8.5-P-R | FDA UDI | Class II | Unknown |
| Paragon | GM08001-349-04 | FDA UDI | Class II | Active |
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