Paragonix announces first pediatric use of BAROguard lung preservation system
October 15, 2024
Paragonix today announced the first pediatric use of its BAROguard Donor Lung Preservation System in a lung transplant case.
Paragonix today announced the first pediatric use of its BAROguard Donor Lung Preservation System in a lung transplant case.
Si-Bone today announced the first patient procedures with its FDA breakthrough device, the iFuse Torq TNT implant system.
Eyenovia (Nasdaq:EYEN) announced that it began manufacturing batches of its Mydcombi product for its next-generation delivery platform.
AtriCure (Nasdaq: ATRC)+
announced that it received CE mark for the EnCompass clamp for cardiac tissue ablation procedures.
Ascensia Diabetes Care announced today that it launched the Eversense 365 CGM system from Senseonics (NYSE:SENS) in the U.S.
Baxter (NYSE: BAX)+
today unveiled its next-generation airway clearance system, The Vest advanced pulmonary experience (APX) system.
Johnson & Johnson MedTech‘s Shockwave Medical today announced the full U.S. launch of its Shockwave E8 peripheral IVL catheter.
FREMONT, Calif., Sept. 10, 2024 /PRNewswire/ — THINK Surgical, Inc., an innovator in the field of orthopedic surgical robots, today announced the successful completion of the first total knee arthroplasty procedure utilizing its new TMINI® Miniature Robotic System version 1.1 following recent FDA 510(k) clearance.
FLOWOOD, Miss., Sept. 10, 2024 /PRNewswire/ — Zavation Medical Products, LLC (“Zavation”), an innovator in spinal device technology, proudly announces the launch of its latest product—the Varisync® ALIF System. Engineered to streamline ALIF procedures, the Varisync system offers customization and efficiency with two spacer fixation options: anchors and screws.
BETHLEHEM, Pa., Sept. 10, 2024 /PRNewswire/ — Tyber Medical LLC, a leading orthopedic device manufacturer specializing in private label implants for the extremity, trauma, and spine markets, is proud to announce that its PEEK ToeGrip Hammer Toe implant family has received Medical Device Regulation (MDR) certification from TÜV Rheinland. This prestigious certification marks the first time a hammer toe implant has achieved both FDA 510(k) clearance and MDR certification, setting a new standard for orthopedic implants.