Origin Medical Devices


Origin Medical Devices is committed to developing next-generation ventilator technology that is accessible to everyone. Their mission is to create high-performance, innovative ventilators that create a paradigm shift in the ventilation market. They focus on reliability, adaptability, and ease of use, aiming to improve patient support and safety while streamlining clinical care.

Industries

health-care
medical
medical-device

Nr. of Employees

small (1-50)

Origin Medical Devices

Newport Beach, California, United States, North America


Products

ICU-grade multi-mode ventilator (high-performance)

A high-performance ventilator platform intended for the sickest patients (neonates to adults) combining invasive ventilation, non-invasive ventilation and high-flow oxygen therapy in a single device without the need for compressed gas.

Portable ICU-performance ventilator

Smaller, more portable ventilator offering ICU-level performance for neonates to adults, designed for operation in challenging environments without compressed gas or proprietary connections.

Value-level portable ventilator

A value-oriented portable ventilator for pediatrics to adults providing ICU-level features with simplified design and lower maintenance demands.

Dedicated non-invasive ventilator with emergency invasive mode

A ventilator focused on non-invasive ventilation use cases that is compatible with a variety of circuits and masks, includes leak management and a dedicated emergency invasive mode.


Services

Quality-focused manufacturing and automated testing

In-house manufacturing approach emphasizing simplified assembly, use of dedicated test fixtures (jigs), and software-driven automated burn-in and verification processes to validate sub-assemblies and final products before release.

Ventilator hardware and software development

End-to-end device development including blower and flow-control hardware design, embedded control and synchrony algorithms, user interface design and integration of respiratory monitoring.

Regulatory and standards compliance management

Management of conformity to medical device directives and standards including ISO 13485, IEC/EN 60601 series, EN 62304 (software lifecycle), EN 62366 (usability) and standards for biocompatibility and respiratory pathway testing.

Expertise Areas

  • Mechanical ventilation system design
  • Critical care and non-invasive ventilation
  • Ventilator software and control algorithms
  • Medical device manufacturing and test automation
  • Show More (4)

Key Technologies

  • Blower-driven ventilation systems
  • Proportional flow-control valves
  • Patient-triggering and synchrony algorithms
  • Volumetric capnography
  • Show More (8)

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