Spine and orthopedic company Medacta celebrated its 25th anniversary in 2024, on top of seeing a 16.2% increase in revenue. Here are eight things to know about Medacta’s 2024 revenue, according to a March 25 news release sent to Becker’s: …
Spinal Tech
Onward’s Arc-IM Lumbar Lead was used in its first human patient, the company said March 26. Dr. Jocelyn Bloch performed the debut case at Lausanne University Hospital (CHUV) in Switzerland, according to a news release. The Arc-IM Lumbar Lead is…
Aurora Spine earned FDA 510(k) clearance for its Aero facet fusion system, the devicemaker said March 25. Aero is a minimally invasive system for facet joint-related pain or instability in levels C2 to S1, according to a news release. It…
Tenon Medical earned FDA 510(k) clearance to use its Catamaran sacroiliac joint system for augmenting thoracolumbar fusion, according to a March 24 news release. With the new indication Catamaran can be used as a standalone treatment or to augment spinal…
SynerFuse is partnering with Velentium Medical to scale the SynerFuse e-TLIF implant, according to a March 21 news release. Velentium Medical will support SynerFuse with strategic development and manufacturing. SynerFuse’s e-TLIF requires one incision and integrates neuromodulation with spinal decompression…
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SurGenTec announced that OsteoFlo HydroFiber, its synthetic bone graft solution equivalent to autograft, is now being used in spinal surgeries following FDA 510(k) clearance. The milestone marks an advancement in bone graft technology, as OsteoFlo HydroFiber is recognized as a…
Here are four spinal devices that have earned FDA approval, as reported by Becker’s since Jan. 24:
The FDA has cleared Spineart’s Perla TL application for use with eCential Robotics Op.nTM robotic navigation platform. The clearance will combine Spineart and eCential Robotics’ robotic-assisted spine surgery technologies, according to a March 13 news release. The new Perla app…
Here are six key updates from spine and orthopedic companies since March 5. 1. Aurora Spine completed enrollment for its Refine study on lumbar interlaminar fusion. 2. Interim data on Spineart’s Baguera-C cervical disc shows the device meets the threshold…
Medtech company Globus Medical has expanded its spine portfolio by launching its Cohere anterior lumbar interbody fusion spacer and Modulus ALIF blades. The Cohere space is the first porous polyether-ether-ketone interbody spacer for anterior lumbar interbody fusion surgery, according to…