Mixed reality surgical training platform apoQlar receives FDA clearance – Mobihealth News
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German company apoQlar announced its plans to raise Series A funding after receiving FDA 510(k) clearance for its VSI HoloMedicine platform, a mixed reality offering that helps surgeons plan for procedures using 3D holographic technology.
The platform enables surgeons to turn radiographic images such as PET, Angio CT, SPECT, CBCT, CT and MRI scans into 3D holograms to examine before surgery.
Through its subsidiary in Miami, Florida, apoQlar will distribute its HoloMedicine platform in the U.S. during the second quarter of 2023, and the prospective Series A raise will help scale its platform.
The Hamburg-based company said it has now received medical certifications in 30 countries.
“With mixed reality, we are no longer bound to physical objects in a physical world. We can leverage digital objects and services on top of the real world for equal or greater utility and usually at a fraction of the cost. Mixed reality is a completely new way for people, and in our case surgeons, physicians and technologists, to continue to experience the real world around them but with an entire virtual layer placed on top,” Sirko Pelzl, cofounder and CEO of apoQlar, said in a statement.
THE LARGER TREND
apoQlar isn’t the only immersive technology platform aiming to help surgeons during the surgery process.
Augmedics’ xvision Spine System, which received FDA clearance in 2019, provides an augmented reality tool that gives surgeons a 3D image of spinal anatomy directly in their line of sight during surgery.
Last year, the Illinois-based company announced it had raised $36 million in Series C funding.
Other immersive tech companies in the surgical training space include London-based virtual reality (VR) surgical training platform FundamentalVR and Sydney-based VR training company Vantari VR.
© 2022 MobiHealthNews is a publication of HIMSS Media
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