Abstract
US ophthalmologic imaging technology company Bioptigen Inc., has received regulatory approval to market its hand-held Envisu C2000-series systems for clinical use within the European Union.
The technology
Bioptigen’s Envisu spectral domain optical coherence tomography imaging systems use low-power, near-infrared light to generate real-time, high-resolution, depth-resolved images of eye structures – equipping researchers and clinicians to explore new avenues of understanding in disease progression, detection and treatment.
Company comments
“Earning a CE Mark is an important milestone for Bioptigen, but it’s even more meaningful for the pediatric and adult patients who now can benefit from our more flexible imaging platform. We bring imaging to the patient; the patient doesn’t have to come to us,” said Dr. Eric Buckland, president and CEO. “Knowing that Bioptigen can improve the quality of life for patients is extremely rewarding.”
Bioptigen’s Envisu C2000 series should prove especially useful for physicians treating non-ambulatory patients, as well as those suffering from conditions such as nystagmus, which causes involuntary eye movement, Buckland added.
“Physicians in Europe play a critical role when it comes to advancing non-invasive medical technologies,” Buckland said. “Bioptigen looks forward to collaborating with these professionals as they develop new best practices based on standards that benefit patients worldwide.”
Source: Bioptigen
published: December 22, 2011 in: Approval/Clearance, News, Ophthalmics