TISSUEMILL TECHNOLOGIES LLC

Tissuemill Technologies LLC specializes in single-use dermatome blades, specifically marketed under the brand name TissueMill. These devices are engineered for precise skin grafting and tissue preparation during surgical procedures, ensuring controlled and accurate cuts for medical applications.

Tissuemill Technologies LLC is headquartered in the United States. The company’s location influences its regulatory compliance and distribution networks, particularly for devices intended for the U.S. market.

The dermatome blades produced by Tissuemill Technologies LLC fall under the classification of Class I medical devices. This classification is typically assigned to devices posing minimal risk to patients, such as those with non-invasive or low-risk procedures, though individual device authorisation still requires compliance with applicable regulations.

Yes, the devices manufactured by Tissuemill Technologies LLC are listed in the FDA Unique Device Identifier (UDI) registry. This registry helps track and identify medical devices in the U.S. market, ensuring transparency and traceability for healthcare providers and regulators.