Placing your orthopaedic and dental devices on the market

As a manufacturer of orthopaedic or dental medical devices, you must ensure that your product meets the relevant regulatory requirements before being placed on the market. It is critical to work with an EU Notified Body or UK Approved Body that understands the industry and has the experience to review and confirm your product’s readiness for market. We truly understand the challenges medical devices manufacturers face in bringing compliant products to market efficiently and safely. We offer a range of flexible product review services providing you with efficient pathways to bring your product to market.

Chris Wylie

Meet our experts

As a manufacturer of orthopaedic and dental medical devices, one of your biggest challenges in breaking into, or continuing your success in, this market is navigating the regulatory process efficiently. Strong, statistically relevant clinical data demonstrating the safety and performance of your device is essential to ensuring a successful outcome of your MDR application.

Our orthopeadic & dental Technical and Clinical Specialists have a broad range of industry and regulatory experience, including product design and development, manufacturing, testing and regulatory expertise. They will support you through the process of certifying your device.

Orthopaedic and Dental