News | Medical 3-D Printing | November 23, 2022

Company takes next major step in providing widespread access to patient-specific 3D models helping healthcare providers deliver precision medicine 

3D-printed anatomic model

3D-printed anatomic model 

 


November 23, 2022 — Ricoh USA, Inc.  announced RICOH 3D for Healthcare has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its craniomaxillofacial (CMF) and orthopedic patient-specific anatomic modeling. 

Find more RSNA22 coverage here 

RICOH 3D for Healthcare is an integrated HIPAA-enabled end-to-end workflow solution for the development, design and production of 3D-printed anatomic models, produced using Stratasys 3D printing technology, that enable healthcare providers to develop patient-specific representations of tissue and bone. 

The precise replicas help clinicians see inside anatomy for greater visibility into patient needs. RICOH 3D for Healthcare integrates with IBM iConnect® Access, an enterprise imaging solution from IBM Watson Health that is used in many hospitals across the U.S., making it easy to integrate into an existing workflow. 

Providers can select from one of two options based on their preferred workstyles or needs. They can choose a point-of-care option, where a Ricoh Managed Services team works onsite at a healthcare facility to manage the entire process using Stratasys 3D printers. Alternatively, healthcare providers can select an on-demand option where they order and have the models printed at a Ricoh facility and shipped directly to them. 

"Ricoh is committed to healthcare innovation that will turn the tide on patient engagement and precision medicine. RICOH 3D for Healthcare does just that—offering a model matched to the unique anatomy of each individual patient," said Gary Turner, Managing Director, Additive Manufacturing, North America, Ricoh USA, Inc. "One of our goals is to address the needs of doctors and patients in specific areas with particularly high demand for 3D-printed anatomic models, the 510(k) clearance for CMF and orthopedic models moves us further toward reaching this goal." 

According to the Radiological Society of North America (RSNA) 3D Printing Special Interest Group, the use of 3D printing technologies to aid clinical care in the CMF area has been in demand from the advent of 3D printing in the late 1980s. Surgeons, engineers and researchers were designing more manual ways of converting medical imaging datasets into 3D models even before the commercialization of 3D printing technologies. 

Patient-specific anatomical models are the baseline in the CMF arena, according to the report, and there is a growing body of work that supports the benefits of 3D-printed models. These include increased comprehension of anatomy and pre-surgical planning for complex surgical cases, as well as a reduction in operation times and improved patient outcomes. 

Ricoh plans to solicit 510(k) clearance for additional treatment regions in the future. 

For more information: www.ricoh.com 


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