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Developments for you

Regardless of whether it is a single component or the entire device: we develop in accordance with ISO 13485 and the associated standards and regulations for medical technology. Supplementary parts or the entire development – you decide which development elements you want us to handle.

  • Development up to Class IIb
  • Hardware and software, mechanical construction
  • Standard-compliant: project management, development process and documentation
  • Assistance with approval procedures

We are an effective partner that stands by your side!