IMM Private Equity is reportedly close to acquiring a controlling stake in CGBio Co., the Korean regenerative medicine company affiliated with Daewoong Pharmaceutical, in a transaction that could value the deal at up to $730 million. According to Korean media reports, IMM PE may acquire as much as 80% of CGBio, following earlier reports that the … [Read More...] about IMM PE Set to Acquire CGBio, Strengthening Korea’s Regenerative Spine Platform
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BREAKING NEWS
Amplio Spine Acquires and Commercializes KeyLift®, an FDA-Cleared Expandable Interlaminar Stabilization System Indicated for Supplemental Fusion of the Non-Cervical Spine
Founder-led Amplio Spine, LLC enters national commercialization following its asset acquisition of KeyLift® from FloSpine, LLC — an FDA-cleared expandable interlaminar device whose Indications for Use specify plate fixation/attachment to the spinous processes/lamina. BOCA RATON, Fla., June 18, 2026 /PRNewswire/ -- Amplio Spine today announced the close of its asset … [Read More...] about Amplio Spine Acquires and Commercializes KeyLift®, an FDA-Cleared Expandable Interlaminar Stabilization System Indicated for Supplemental Fusion of the Non-Cervical Spine
Amber Implants Advances Pivotal European EXPAND Study of VCFix® Spinal System in Standalone Vertebral Reconstruction
Study evaluates VCFix® used with or without bone cement, expanding clinical experience with the company’s minimally invasive spine platform. The Hague, Netherlands, June 17, 2026 (GLOBE NEWSWIRE) -- Amber Implants, a medical technology company redefining vertebral fracture treatment through minimally invasive reconstruction and targeted stabilization, today announced the advancement of its … [Read More...] about Amber Implants Advances Pivotal European EXPAND Study of VCFix® Spinal System in Standalone Vertebral Reconstruction
Mighty Oak Medical Receives FDA Clearance for Acorn 3D™ Pre-Surgical Planning Platform
Mighty Oak Medical is excited to announce the latest 3D pre-surgical planning software FDA clearance: 𝗔𝗰𝗼𝗿𝗻 𝟯𝗗™ spinal deformity correction planning! Powered by AI-driven automated scan segmentation and pre-correction measurements, 𝗔𝗰𝗼𝗿𝗻 𝟯𝗗™ enables a user to, among other things, visualize the simulated corrected spine versus the pre-corrected spine. Spinal deformity correction is a 3D problem, … [Read More...] about Mighty Oak Medical Receives FDA Clearance for Acorn 3D™ Pre-Surgical Planning Platform
SurGenTec® Receives FDA Clearance for ION-L™, a Novel Lumbar Facet Fixation System Representing a Paradigm Shift in Minimally Invasive Spine Surgery
BOCA RATON, Fla.--(BUSINESS WIRE)--SurGenTec®, a medical device company focused on advancing treatment options for orthopedic and spine surgery, today announced FDA clearance of its ION-L™ Lumbar Facet Fixation System. ION-L™, part of SurGenTec's facet fixation platform, is indicated for the treatment of patients with degenerative disc disease (DDD) from L3 to S1 in skeletally mature patients who … [Read More...] about SurGenTec® Receives FDA Clearance for ION-L™, a Novel Lumbar Facet Fixation System Representing a Paradigm Shift in Minimally Invasive Spine Surgery
Percutaneous MIS Spine Systems: Why Adoption Still Lags 25 Years After Sextant
When Medtronic put Sextant on the market at the start of the 2000s, percutaneous pedicle screw fixation looked like the obvious endpoint for lumbar surgery: the same construct, a fraction of the soft-tissue damage. Nearly a quarter-century later, that endpoint has only partly arrived. MIS spine has been one of the most promising stories in the implant market for years. The technology is better, … [Read More...] about Percutaneous MIS Spine Systems: Why Adoption Still Lags 25 Years After Sextant
Why the Locals Win in Brazil | Updated 2026
Almost everywhere, spine belongs to the multinationals. Brazil doesn't follow the script, and the reasons run deeper than price. Run down the top of the spine market in the US, Europe or most of Asia and the same names keep showing up: Medtronic, DePuy Synthes, Stryker (VB Spine) , Globus Medical. Brazil is the odd one out. The biggest slice of the market there belongs to domestic companies … [Read More...] about Why the Locals Win in Brazil | Updated 2026
L&K Spine Performs First U.S. Deformity Case With BluEX-LT Curved Expandable Cage
L&K Spine has reported the first human clinical use of its BluEX-LT curved expandable lateral cage in a spinal deformity procedure performed in the United States. The case was completed at WakeMed Health & Hospitals in North Carolina and represents an important clinical milestone for the company’s U.S. expansion strategy. The procedure involved a patient with significant spinal … [Read More...] about L&K Spine Performs First U.S. Deformity Case With BluEX-LT Curved Expandable Cage
SpinaFX Medical receives FDA Investigational Device Exemption (IDE) for Triojection®, its Breakthrough, Minimally-Invasive, Image-Guided Lumbar Disc Treatment.
The prospective, randomized, multicenter trial will compare intradiscal ozone/oxygen injection plus nerve root block to nerve root block alone in 300 patients in up to 30 US sites TORONTO, June 9, 2026 /PRNewswire/ - SpinaFX Medical, a clinical-stage medical device company specializing in minimally invasive, image-guided therapies for intravertebral disc disorders, today announced … [Read More...] about SpinaFX Medical receives FDA Investigational Device Exemption (IDE) for Triojection®, its Breakthrough, Minimally-Invasive, Image-Guided Lumbar Disc Treatment.
Xenix Medical Announces FDA Clearance and Full Commercial Launch of the Lux™ Expandable Lumbar Interbody Fusion System
Expandable Design Incorporates the Company’s NanoACTIV™ Surface and NeoWave™ Structure Technologies to Enhance the Potential for Fusion While Minimizing the Risk of Subsidence ORLANDO, Fla.--(BUSINESS WIRE)--Xenix Medical today announced FDA 510(k) clearance and full commercial launch for its Lux Expandable Lumbar Interbody Fusion System. Lux is the result of strong market demand for an … [Read More...] about Xenix Medical Announces FDA Clearance and Full Commercial Launch of the Lux™ Expandable Lumbar Interbody Fusion System
Life Spine Announces Update in ProLift® Patent Case
The case began in 2021, when Globus filed a lawsuit alleging that Life Spine’s ProLift® product line infringed certain Globus patents. During the proceedings, Life Spine challenged the patentability of several asserted patents. In 2024, the United States Patent Trial and Appeal Board cancelled all claims from four patents that Globus had asserted against Life Spine. The remaining claims … [Read More...] about Life Spine Announces Update in ProLift® Patent Case
FDA Grants 510(k) Clearance for Pulmera’s CBeam™ 3D Imaging Platform
Palo Alto, CA, June 02, 2026 (GLOBE NEWSWIRE) -- Pulmera, an emerging medical technology company developing next-generation intraoperative imaging solutions, today announced that it has received U.S. Food and Drug Administration 510(k) clearance for its CBeam™ 3D imaging platform. CBeam is designed to transform conventional 2D surgical C-arms into intraoperative 3D imaging systems, helping … [Read More...] about FDA Grants 510(k) Clearance for Pulmera’s CBeam™ 3D Imaging Platform