BUENA, N.J., May 29, 2024 /PRNewswire/ — COMAR, a leading provider of innovative medical devices and packaging solutions, is thrilled to announce a significant achievement. After rigorous preparation, they successfully obtained their CE certificate under the latest EU Medical Device Regulations (EU MDR 2017/745).

HALO AP Dx brings digital primary diagnosis to anatomic pathology labs in the US.

Canary Medical announced today that it received FDA breakthrough device designation for its Canturio lumbar cartridge.

Medtronic (NYSE: MDT)+
announced today that the FDA granted breakthrough device designation for its Infuse bone graft.