Carestream’s OnSight 3D Extremity System Gets FDA 510(k) Clearance

Carestream, part of the Onex family of companies based in Canada, receive FDA 510(k) clearance and is available for order in the U.S. market.

This device enables healthcare providers to capture 3D images and conduct a patient consultation in a single visit. Patients are also able to view 3D images that illustrate their condition or injury.

This new imaging system will be demonstrated at the American Society for Surgery of the Hand (ASSH) conference that begins on Sept. 29. — Cynthia Jessup