Medeon Biodesign is pleased to announce that its innovative laparoscopic port site closure device, AbClose™, successfully closed more than 50 wounds in a variety of laparoscopic surgeries. The device consistently demonstrated its simplicity, stability and predictability in the hands of multiple physicians in an ongoing pre-commercial clinical evaluation in the United States. The U.S. Food and Drug Administration 510(k) cleared …

Diagnostic Medical Systems SA Signs Distribution Agreement For Its Lipofilling Solution In China And Taiwan With Chinese Highfive Biotech Company. Signs Distribution Agreement Through Its Subsidiary DMS Biotech With Highfive Biotech Company. This Agreement Guarantees A Minimum Turnover Of 5.7 M € Over Five Years For DMS Biotech‍.

Orion Health™ has signed a five-year contract with Integrated Health Information Systems (IHiS), the health technology agency for Singapore, for the delivery of a Singapore-wide deployment of a Healthcare Enterprise Service bus, powered by the company’s flagship interoperability solution, Rhapsody Integration Engine™. Rhapsody will deliver the interoperability services and infrastructure for the public hospitals comprising the National Electronic Health Record …

At the 24th Congress and General Assembly of the International Union of Crystallography (IUCr), Bruker and DECTRIS today announce the EIGER2 R 500K, the latest generation of Hybrid Photon Counting (HPC) pixel detectors developed by DECTRIS, the technology leader for HPC detectors for laboratory instrumentation and synchrotron beam lines. In close collaboration, DECTRIS and BRUKER have seamlessly integrated this outstanding …

Genesis Healthcare Co. has announced the completion of a new share issue worth 1.4 billion yen for allotment to Rakuten Inc. Furthermore, Rakuten’s Chairman and CEO will join Genesis Healthcare’s Board of Directors as an External Board Director. As a result of the new stock offering, Genesis Healthcare’s capital has increased to 2.1 billion yen, one of the largest paid-in-capital …

Vertera Spine announced the COALESCE™ Lumbar Interbody Fusion Device has received U.S. Food and Drug Administration (FDA) 510(k) clearance for use in anterior, transforaminal, posterior, and lateral lumbar interbody fusion procedures. COALESCE features Vertera Spine’s novel proprietary porous PEEK biomaterial and is the second porous PEEK device to receive FDA clearance behind Vertera Spine’s COHERE® Cervical Interbody Fusion Device. Vertera …

Globally, CVD is the number 1 cause of death; which represents 30% of global death. Kinpo Electronics Inc. provisioned future burden caused to people. Being one of the top EMS manufacturers, Kinpo Electronics Inc. has developed a solution for CVD prevention. Today they proudly announced acquirement of medical CE MDD certificate for its in-house developed wearable ECG monitor, BC1 Patch. …

Varian Medical Systems, announced it has been selected through its distributor, Business Alignment, to supply and install a Varian ProBeam® Compact single-room proton therapy system in the oncology center at King Chulalongkorn Memorial Hospital in Bangkok, Thailand. First patient treatments are expected to start in the second half of 2019. In addition to the equipment, Varian will also provide its …

Seegene Inc. announced that it has entered into a new strategic collaboration relationship with Thermo Fisher Scientific in which Seegene will file for U.S Food and Drug Administration (FDA) clearance of its Allplex™ diagnostic assay portfolio at the same time that Thermo Fisher files for FDA clearance to run Seegene’s assays on Thermo Fisher’s QuantStudio™ 5 Real-Time PCR System (PCR …

Dr. Ralph Mobbs of the Neuro Spine Clinic completed the procedure on April 28, 2017 at the Prince Of Wales Private Hospital. The procedure was performed on a 46-year-old male patient suffering from a degenerative cervical disc at level C6-C7. The patient failed conservative treatments prior to undergoing surgery. The AxioMed viscoelastic disc is a next-generation disc replacement that restores …