EAGLEGRID® 2.0 is the digital revision of the previous iuxta-bone implant. Thanks to new technologies, this medical device, already compliant with the new European directive on implantology of 2020, solves all those cases of severe atrophy of the upper jaw or mandible where the residual bone does not allow the use of endosseous implants. Its extreme precision along with the patient’s receiving cortical bone is then improved by stabilization by means of appropriate synthesis screws, which will the EAGLEGRID® 2.0 the certainty of bone integration.
EagleEgrid® 2.0 is a customized medical product that complies with the requirements of directive 93/42/EEC and 2017/745/EEC. The manufacturers is correctly registered in the Register of manufacturers of made to-measure medical devices legitimately operating in Italy under the jurisdiction of the Ministry of Health.