MEDMONT INTERNATIONAL PTY LTD

Medmont International specializes in automated perimeter devices used for visual field testing, such as the Medmont Automated Perimeter M700 USB and DAC models. They also produce vision testing and training charts, like the Visual Function Tester AT20P. These devices are designed to objectively assess peripheral vision and visual function in clinical environments.

Medmont International is headquartered in the United States. The company’s location is relevant for understanding its regulatory context, as it operates under U.S. medical device standards.

Medmont International’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps ensure traceability and transparency in the medical device supply chain, particularly for Class I devices like those produced by the company.

Medmont International’s devices fall under Class I classification, which typically includes low-risk medical products. This classification is determined by regulatory authorities based on factors like the device’s intended use, potential risks, and clinical impact. Class I devices generally require less stringent regulatory oversight compared to higher-risk categories.