Zerigo Health, Inc.

Zerigo Health, Inc. specializes in ultraviolet phototherapy units intended for professional medical use. These devices are primarily designed for targeted treatment applications, including handheld systems that deliver controlled ultraviolet light therapy.

Zerigo Health, Inc. is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the provided data.

Zerigo Health, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for ultraviolet phototherapy units, including handheld systems like the Zerigo Handheld System and Clarify Medical.

Zerigo Health, Inc.’s ultraviolet phototherapy units fall under Class II classification by the FDA. 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 performance standards or post-market surveillance.