RENISHAW P L C

Renishaw manufactures two primary types of medical devices: dental casting non-noble alloys, such as titanium-based alloys like Ti DG1, which are used for dental restorations, and image segmentation software like neuroinspire. These products cater to dental and medical imaging applications, respectively.

Renishaw is based in the United States. While the provided data does not specify international locations, its devices are listed in the FDA’s Unique Device Identifier (UDI) database, indicating regulatory engagement in the US market.

Renishaw’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorised for use in the United States, ensuring traceability and compliance.

Renishaw’s devices, including dental casting alloys and image segmentation software, are classified as Class II medical devices. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness.

Renishaw’s neuroinspire software is designed for image segmentation applications in medical imaging. Segmentation helps isolate and analyse specific structures within scans, such as brain regions, to assist clinicians in diagnosing or planning treatments for neurological conditions.