MEDROCK, INC

MEDROCK, INC makes external manual massagers for clinical use, such as the HotRock device. These products are designed to provide massage therapy and are used in clinical settings. The company's portfolio is regulated as Class I devices, which means they are subject to general controls but do not require premarket approval.

MEDROCK, INC is based in the United States (US). This information is provided directly in the device data, which specifies the company's country as US. The location is relevant for understanding the regulatory jurisdiction under which its devices are listed and monitored.

MEDROCK, INC's devices are listed in the FDA UDI registry. This is explicitly stated in the device data under 'LISTED IN: fda_udi'. The FDA UDI system tracks medical devices sold in the United States, and inclusion means the company has submitted device identifier information for its products, such as the HotRock, as required by regulation.

MEDROCK, INC's devices are classified as Class I. This classification is specified in the device data under 'DEVICE CLASSES: Class I'. Class I devices are subject to general controls and are considered low risk, which aligns with the nature of external manual massagers used in clinical settings for massage therapy.