STOCKHOLM, Dec. 12, 2019 /PRNewswire/ — In the latest version of Ortoma Treatment Solution, OTS 4, Ortoma has introduced support of Artificial Intelligence. The system drastically reduces the time needed for pre-operatively planning of a hip implant in 3D, which has created a big interest for the company’s unique solution. Performance has been a focus area during the …
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WINNIPEG, MANITOBA (PRWEB) DECEMBER 11, 2019 The Orthopaedic Innovation Centre Inc. (“OIC” or “the Company), a non-profit centre for medical device testing and research and development, announced today the release of a featured article in Spinal Surgery News detailing implant fixation in lumbar spinal fusion. Spinal fusion is indicated as a surgical remedy for degenerative and …
December 10, 2019 MEMPHIS, Tenn.–(BUSINESS WIRE)–In2Bones Global, Inc. today announced the global launch of the AlloAid BioNail™, an engineered, sterile allograft implant designed to provide rigid, stable fixation during reconstructive surgery of the hand and foot. Derived from strong cortical allograft, the AlloAid BioNail provides osteoconductive properties to encourage bone remodeling and healing, thus enabling a more …
December 10, 2019 BEDFORD, Mass.–(BUSINESS WIRE)–Anika Therapeutics, Inc. (NASDAQ: ANIK), a global, integrated joint preservation and regenerative therapies company with products leveraging its proprietary hyaluronic acid (HA) technology platform, today announced it will commence the full U.S. commercial launch of TACTOSET, its surgically delivered therapy for bone repair procedures, at the Orthopaedic Summit 2019: Evolving Techniques (OSET), …
HOLLAND, Mich., Dec, 10, 2019 /PRNewswire/ — Shoulder Innovations, (SI), a leading innovator in the development of shoulder replacement systems, announced today that they have received FDA clearance for their InSet Plus™ augmented glenoids for the InSet™ Total Shoulder System. The InSet™ Total Shoulder System is used to treat significant disability in degenerative, rheumatoid and traumatic disease of the …
SALT LAKE CITY, Dec. 10, 2019 /PRNewswire/ — OrthoGrid Systems, Inc., a global medtech leader in alignment technology for orthopedic surgery, announces today that its newest application, PhantomMSK Trauma, has received 510(K) clearance from the U.S. Food and Drug Administration (FDA). OrthoGrid Systems’ PhantomMSK is a universal software platform that works with all manufacturer devices across multiple procedures …
UDINE, Italy, Dec. 9, 2019 /PRNewswire/ — LimaCorporate is pleased to announce the FDA 510K approval for Smart SPACE Shoulder 3D Planner & 3D Positioner. Smart SPACE is an innovative digital platform developed by TechMah Medical thanks to collaboration with LimaCorporate, who entered into a milestone-based acquisition agreement last year. TechMah Medical was founded by Dr. Mohamed Mahfouz, Professor of Biomedical Engineering …
BETHLEHEM, Pa., Dec. 9, 2019 /PRNewswire/ — Tyber Medical, LLC, a manufacturer of private label orthopedic and spinal implants, ranked No. 2 on the list of fastest growing companies in the Lehigh Valley by Lehigh Valley Business, held a ribbon cutting ceremony today to celebrate the official opening of its new state-of-the-art, vertically-integrated, medical device manufacturing facility. The ribbon cutting …
KFAR SABA, Israel, Dec. 9, 2019 /PRNewswire/ — CartiHeal, developer of Agili-C™, a proprietary implant for the treatment of cartilage lesions in arthritic and non-arthritic joints, announced today that the external and independent Endpoint Adjudication Committee (EAC) performed the first Interim Analysis (IA) on the study data following enrollment of the 250th Subject into the study. The EAC reviewed …
KFAR SABA, Israel, Dec. 9, 2019 /PRNewswire/ — CartiHeal, developer of Agili-C™, a proprietary implant for the treatment of cartilage lesions in arthritic and non-arthritic joints, announced today that the external and independent Endpoint Adjudication Committee (EAC) performed the first Interim Analysis (IA) on the study data following enrollment of the 250th Subject into the study. The EAC reviewed …
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