Capabilities

>Capabilities

Reshaping the Medical Device Paradigm

Actuated Medical Inc. has quickly emerged as a leader in designing and developing next-generation, FDA-compliant medical devices. All of our products have one thing in common: Innovative Motion™, a revolutionary actuation technology that is reshaping the traditional healthcare model.

From the creative innovators who work here, to our ISO-certified quality control system, we offer the medical industry and our OEM partners the very best in experience, expertise, and working relationships. Whether you are looking for state-of-the-art devices and components, high-tech and high-quality models and prototypes, or a great partner to help you move your idea from concept to FDA approval, look no further.

Innovative motion. Positive outcomes… for patients, health care providers, and our partners.

Innovative Products

Actuated Medical scientists and product development experts design, develop, and manufacture FDA-compliant medical devices and components to meet patients' and clinicians' diverse needs. All of our products use Innovative Motion™ technology and are designed, tested, and manufactured under an ISO-certified quality control system. Our products include Occlusion Clearing Systems, Controlled Tissue Penetration Systems, and MRI Compatible Systems.

Comprehensive Services

Actuated Medical has a proven track record of receiving federal grant monies to develop successful and effective medical devices and components. We partner with OEMs from the concept phase to FDA-approval, and we can assist with Outsourced R&D, Modeling, Prototyping, and Manufacturing.

Sound Partnerships

When you partner with Actuated Medical, you’re leveraging the power of experience and expertise. Our business model is to:

  • Develop a product.

  • Obtain FDA approval.

  • Scale up manufacturing.

  • Hand off large-scale manufacturing to contract manufacturers.

From concept to development, the process is managed by an exceptional team of:

  • Engineers

  • Scientists

  • Medical device clinical advisors

  • Quality assurance and regulatory experts

When Actuated Medical develops a device using SBIR grants we take it through Phase II. In this situation, it takes an average of three years to have a device ready for clinical trials. At the conclusion of Phase II, Actuated Medical licenses the IP to an OEM with market share. The IP license will depend on issues such as the market size, territory, and the agreement between Actuated Medical and the OEM.

We also work in partnership with strategic companies using federal grants to fund our R&D. Working to the OEM's specifications, we develop grant proposals and submit them to the appropriate agency. An OEM team member is included on the proposal to ensure the device meets that OEM's design specifications. Once feasibility and bench top prototyping is complete, the OEM has the option to license the IP via a follow-on agreement.

Call us 814–355–0003  l  Email us info@actuatedmedical.com
310 Rolling Ridge Drive  l  Bellefonte, PA 16823

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