2742 results found.
Creative Medical Launching StemSpine Stem Cell Treatment in the U.S.
Creative Medical Technology will begin U.S. commercialization of StemSpine®, a regenerative stem cell procedure for the treatment of degenerativ...
CarboFix Gains FDA Clearance for Carbon Fiber VBR
CarboFix received FDA 510(k) clearance to market CarboClear® Carbon Fiber Vertebral Body Replacements.
Safe Orthopaedics Reports 3Q19 Revenue of EUR 1.2MM, +40.8% vs. 3Q18
Safe Orthopaedics reports 3Q19 orthopedic revenue of EUR 1.2MM (USD $1.3MM), +40.8% vs. 3Q18.
DePuy Synthes Reports 3Q19 Revenue of $2,137, +1.2% vs. 3Q18
DePuy Synthes reported 3Q19 orthopedic revenue of USD $2,137MM, +1.2% vs. 3Q18.
Spineway Mont Blanc MIS Approved in Japan
Spineway obtained regulatory approval in Japan for its Mont Blanc minimally invasive surgical devices.
Zimmer Biomet Launches TrellOss-TC Porous Titanium Interbody System
Zimmer Biomet launched the TrellOss™-TC Porous Titanium Interbody, completing its initial offering of porous titanium implants.
Aegis Spine Gains FDA Clearance for AccelFix Expandable Cage
Aegis Spine received FDA 510(k) clearance to market the AccelFix Expandable Cage System.
Viseon's First Clinical Use of Voyant Lateral System
Viseon announced the first clinical use of Voyant Lateral visualization to support real-time imaging during a minimally invasive lateral lumbar procedure.
Amplify Surgical Announces 100th Level Treated with dualX Expanding Interbody
Amplify Surgical marked the milestone of 100 surgical levels implanted with the dualX™ Expanding Interbody Fusion System.
Spineology Raises $7MM in Equity
Spineology raised $7MM of a potential $16MM round of equity funding.
Centinel Spine Marks 18 Years of prodisc L Use in the U.S.
Centinel Spine announced the milestone of the 18th year of clinical usage of prodisc® L in the U.S.
Epica Gains FDA Clearance for SeeFactorCT3
Epica was granted FDA 510(k) clearance to market the SeeFactorCT3™ Imaging Platform, comprising computed tomography, fluoroscopy and digital radiography in one syst...
Back 2 Basics Gains FDA Clearance for Carbon Interbody Cages
Back 2 Basics received FDA 510(k) clearance to market eCarbon anterior cervical and posterior lumbar Interbody devices.
DeGen Medical Gains New FDA Clearances
DeGen Medical received FDA clearance to market the F1 MPS™ Modular Pedicle Screw System for JOUST™ Minimally Invasive Surgery and the Cyclops™ Anterior Cer...
Medical Device Industry Stakeholders Seek Permanent Repeal of Medical Device Tax
The Medical Device Manufacturers Association, the Advanced Medical Technology Association, the Medical Imaging & Technology Alliance and numerous industry stakeholders are
DiscGenics IDCT Study Update
Preclinical study results demonstrated that intradiscal injection of Discogenic Cells, the active ingredient in DiscGenics' IDCT allogeneic cell therapy, may be a viable treatment for ...
4WEB Medical Completes Cell Differentiation and Gene Expression Study
4WEB Medical completed Phase I in vitro testing to demonstrate that surface roughness on its 3D-printed truss implants stimulates a superi...
SpineWelding Gains FDA Clearance for Elaris Pedicle Screw
SpineWelding received its first FDA 510(k) clearance, addressing the Elaris Pedicle Screw.
CTL Amedica Debuts MONET Integrated ACIF Cage
CTL Amedica launched the MONET™ ACIF Integrated Cage with supplementary fixation.
Brainlab Introduces Loop-X Mobile Intraoperative Imaging Robot
Brainlab unveiled Loop-X™, reported to be the first mobile intraoperative imaging robot.
RTI Surgical Launches CervAlign Anterior Cervical Plate
RTI Surgical commenced full commercial launch of the CervAlign® Anterior Cervical Plate following successful limited release.
Biedermann Motech Expands its iMAS360 Procedural Solution
Biedermann Motech integrated the DELTA XS™ Shank Based Retractor into the iMAS360™ lumbar fusion procedure.
SI-BONE 5-Year iFuse Study Results
SI-BONE reports that 5-year follow-up from studies of the iFuse implant for SI joint fusion showed excellent durability of clinical responses and positive radiographic outcomes...
Life Spine Gains FDA Clearance for Hinged Laminoplasty System
Life Spine was granted FDA 510(k) clearance to market a Hinged Laminoplasty System.
Medtronic Initiates Clinical Trial for Infuse Bone Graft in TLIF
Medtronic commenced site recruitment in a prospective, randomized pivotal clinical trial on the use of Infuse™ Bone Graft in TLIF.
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