Signature Orthopaedics offers a complete range of services to take your ideas from conception, into production and market release. Our in-house resources feature state of the art product development tools, such as CAD software, finite element analysis and direct translation of MRI/CT data into CAD space to generate patient matched implants and instruments.

Signature Orthopaedics can take an engineering concept and manufacture first article prototypes that can be tested per ISO / FDA testing requirements on our in-house MTS test frames. This capability ensures rapid product development cycles and results in earlier market release.

Our engineering and regulatory expertise ensures that complex production processes are validated and achieve regulatory approval. We have a proven track record in achieving regulatory approval of medical devices, meeting the stringent requirements of both the European MDD and the US FDA regulatory systems. Signature Orthopaedics has its own in-house regulatory and clinical support services that ensure we meet all post market surveillance requirements to ensure product compliance. Working closely with orthopaedic companies, we are able to help develop specific devices rapidly for all markets.