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Saluda Medical earns FDA approval for automated SCS platform
Saluda Medical earned FDA approval for its biomarker-based automated patient programming platform used in spinal cord stimulation. -
How 3D spine implants are shaking up the future of surgery
As technology continues to advance, so too does the possibility of better outcomes in spine surgery. -
Centinel Spine's disc replacement sales grow 38% in 2024: 6 notes
Centinel Spine saw prodisc revenue surpass $95 million in 2024, according to a Jan. 23 news release. -
Aurora Spine promotes 2 executive leaders
Aurora Spine promoted two executive leaders, the spine devicemaker said Jan. 22. -
5 medtech notes: Medtronic, Johnson and Johnson and more
From new leadership to product launches, here are five key updates from spine and orthopedic devicemakers since Jan. 15. -
Osteotec, Highridge Medical form spine surgery partnership
Medical device manufacturer Osteotec has reached an exclusive distribution agreement with Highridge Medical in the U.K. -
Orthofix CFO sells $83K in stock
Julie Andrews, Orthofix's CFO, sold 4,655 shares of common stock on Jan. 16, according to a Jan. 21 SEC filing. -
SI-BONE announces Posteromedial Trajectory
SI-BONE (NASDAQ: SIBN) has introduced an advanced posteromedial technique for its iFuse TORQ® Implant System, expanding its suite of minimally invasive solutions for treating sacroiliac joint (SIJ) dysfunction. Developed in partnership with Dr. Babajide Ogunseinde from Longview, Texas, the posteromedial technique offers a streamlined approach to treating SIJ dysfunction that enables surgeons to address both SI joints through a single midline incision, with one surgical position. This innovation aims to improve efficiency in the operating room by simplifying the procedure for spine surgeons and interventional spine specialists. -
Medtronic names new CFO
Medical devicemaker Medtronic has appointed Thierry Piéton as CFO. -
7 spine, orthopedic devices earning FDA clearance in 1 month
Here are seven orthopedic and spine devices and technologies that have recently received FDA clearance, as reported by Becker's since Dec. 17: -
5 medtech notes: Onward, Icotec and more
From device clearances to mergers, here are five developments from spine and orthopedic devicemakers since Jan. 8. -
Icotec earns FDA clearance for BlackArmor spine implants
Spine devicemaker icotec earned FDA 510(k) clearance for its BlackArmor spine implants, according to a Jan. 14 news release. -
Saluda Medical closes $100M financing
Saluda Medical closed a $100 million finance round, the spine company said Jan. 10. -
Onward's first Arc-EX systems sold in the US
Onward Medical's Arc-EX spinal cord stimulator saw its first U.S. sales in late December, according to a Jan. 9 news release. -
4 medtech notes: Medtronic, Stryker and more
From new partnerships to acquisitions, here are four key developments from spine and orthopedic medtech companies since Jan. 1. -
Stryker to acquire medical device company for $4.9B
Stryker has entered a definitive agreement to acquire medical device company Inari Medical for approximately $4.9 billion. -
SpineGuard, Omnia Medical extend partnership
SpineGuard and Omnia Medical extended their partnership and have their eyes on U.S. market growth, according to a Jan. 6 news release. -
Breakthrough in Spine Surgery: 3,000th Level Implantation of PathLoc-TM, PLIF/TLIF Expandable Cage
L&K Spine Inc. is thrilled to announce a landmark achievement in the field of spinal surgery with the 3,000th successful level implantation of its flagship product as of December 27, 2024, the PathLoc-TM PLIF/TLIF Expandable Cage. This cutting-edge spinal implant represents a transformative advancement in personalized surgical solutions for spinal disorders, offering unparalleled adaptability and precision. -
Stryker in Q4: 5 headlines to know
Here are five updates to know on medtech company Stryker that Becker's reported on during the fourth quarter: -
Onward's spinal cord stimulator earns FDA nod
Onward's Arc-Ex spinal cord stimulator earned the FDA's de novo classification and U.S. market authorization, according to a Dec. 19 news release.
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