REVENIO’S NEW FUNDUS IMAGING DEVICE AUTHORIZED FOR SALE IN THE UNITED STATES AND EUROPE
Revenio Group Corporation Press release December 9, 2019, at 9:00 am EETDRSplus, the newest addition to CenterVue’s family of fundus imaging devices, has been approved by the Food and Drug Administration in the USA and CE certified in Europe. This means that the sales and marketing of the new product will start in 2019 in Europe and early 2020 in the United States. Revenio acquired CenterVue in April 2019. First launched in 2011, CenterVue’s widely successful DRS device will gradually be replaced by the DRSplus model which is especially well suited for the evaluation of diabetic