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Company's VSP solutions span craniomaxillofacial, orthopedics, and now expanded adolescent applications.
January 14, 2026
By: Michael Barbella
Managing Editor
3D Systems has secured U.S. Food and Drug Administration (FDA) 510(k) clearance for expanded indications to its VSP Orthopedics virtual surgical planning and patient-specific instrumentation platform. The planning tool now includes skeletally mature adolescents of normal bone stature, besides adults.
Key investment highlights include:
“This regulatory clearance removes a significant friction point for adoption in the pediatric/adolescent orthopedic oncology segment,” said Ben Johnson, senior vice president of medical technology at 3D Systems. “Surgeons have been using off-label or compassionate use solutions for years; this decision immediately converts those cases into routine clinical practice and opens the U.S. adolescent bone sarcoma and deformity market to our platform. We are thrilled to now offer these solutions to an expanded and underserved patient population.”
This regulatory clearance further supports 3D Systems’ focus on high-margin personalized healthcare solutions amid ongoing segment optimization efforts. Continuing expanded indications provides a meaningful tailwind for sustaining double-digit average annual growth in the healthcare segment, driven in part by accelerated adoption in this discrete, high-value market.
For nearly 40 years, Chuck Hull’s curiosity and desire to improve the way products were designed and manufactured gave birth to 3D printing, 3D Systems, and the additive manufacturing industry. Since then, that same spark continues to ignite the 3D Systems team as it works with customers to change the way industries innovate. As a full-service solutions partner, the firm delivers 3D printing technologies, materials, and software to high-value markets such as medical and dental; aerospace, space and defense; transportation and motorsports; AI infrastructure; and durable goods.
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