EQUIDOR MEDTECH LLP

EQUIDOR MedTech LLP specializes in posturography systems, which are used to evaluate balance and stability by analyzing body movements and positional control. Their primary device, EQUIPOISE, focuses on clinical assessments of vestibular and neurological conditions through dynamic stability testing.

EQUIDOR MedTech LLP is headquartered in the United States. The company’s location is relevant for understanding its regulatory and operational context, particularly in relation to FDA compliance and market distribution.

EQUIDOR MedTech LLP’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to verify device details.

EQUIDOR MedTech LLP’s devices fall under the FDA’s Class I regulatory category. This classification is typically assigned to low-risk devices that pose minimal potential harm to users, often requiring less stringent premarket review compared to higher-risk classes.