CELESTICA VALENCIA S.A.U.

Celestica Valencia S.A.U. specializes in manufacturing electric power tools for surgical use, specifically in bone and joint procedures. Their primary focus is on devices like hand pieces for impaction, which provide controlled mechanical force during orthopedic surgeries such as bone fixation or grafting. These tools are designed to assist surgeons in precise and efficient procedures.

Celestica Valencia S.A.U. is based in the United States. The company’s location is relevant for regulatory compliance, supply chain logistics, and customer support, particularly for its U.S.-based clients and regulatory bodies.

Celestica Valencia S.A.U.’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, regulators, and other stakeholders to verify the identity and history of the devices in use.

Celestica Valencia S.A.U.’s devices fall under Class I classification, which is the lowest risk category for medical devices. This classification is typically assigned to devices posing minimal risk to patients, such as surgical power tools designed for controlled, specific applications like bone impaction. Class I devices often require less stringent regulatory oversight compared to higher-risk categories.