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Sign in to claim this brandMEDICAL MANUFACTURERS PTY LTD
US
Last updated May 31, 2026
What MEDICAL MANUFACTURERS PTY LTD makes
Medical Manufacturers Pty Ltd produces low-level laser therapy devices designed for home use in musculoskeletal and physical therapy applications. These devices are intended to deliver targeted laser treatment for conditions such as joint pain, muscle recovery, and soft tissue injuries.
The company’s portfolio is classified under FDA’s Class II regulatory category and is listed in the FDA’s Unique Device Identifier (UDI) database. The devices are manufactured in 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 Medical Manufacturers Pty Ltd specialize in?
Medical Manufacturers Pty Ltd specializes in low-level laser therapy devices designed for home use. These devices fall under the musculoskeletal and physical therapy category, specifically targeting conditions like joint pain, muscle recovery, and soft tissue injuries. The focus is on delivering laser treatment in a home setting, making them accessible for self-administered therapy.
Where is Medical Manufacturers Pty Ltd based, and where are their devices manufactured?
Medical Manufacturers Pty Ltd is based in the United States. The company’s devices, including the low-level laser therapy systems, are manufactured in the US. This aligns with the regulatory and operational context provided for their product portfolio.
Which regulatory registries or databases list Medical Manufacturers Pty Ltd’s devices?
Medical Manufacturers Pty Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for devices classified under the FDA’s regulatory framework, specifically for Class II devices.
How are Medical Manufacturers Pty Ltd’s devices classified under FDA regulations?
Medical Manufacturers Pty Ltd’s devices are classified under the FDA’s Class II regulatory category. This classification is typically assigned to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as low-level laser therapy systems for musculoskeletal therapy.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 759484392
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ltu-904 | LTU-904 | FDA UDI | Class II | Active |
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