14541 results found.
                    
Member Success Story: Marty Altshuler Shares Lessons Learned in Building a Spine Company
 
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Garwood Medical Granted FDA Breakthrough Device Designation for Biofilm Tool
Garwood Medical Devices was granted a Breakthrough Device designation from FDA for BioPrax™, an electrical stimulation tool to help eliminate ...
Nanovis Gains FDA Clearance for Bioceramic Nanotube Surface
Nanovis received the first FDA 510(k) clearance for a bioceramic nanotube surface that demonstrates FDA's requirements for nanotechnology.
ARTEBONE Patent Application Accepted in Canada
BBS-Bioactive Bone Substitutes' patent application regarding a bone protein preparation has been accepted in Canada.
Implanet Granted Patent in Japan for JAZZ Lock
Implanet was granted a patent in Japan for JAZZ Lock® technology, part of its JAZZ™ solutions platform to treat degenerative spine disorders.
Alphatec Launches IdentiTi for Lateral Interbody Fusion
Alphatec launched IdentiTi™ porous titanium implants for lateral interbody fusion procedures.
Synaptive Medical Collaborates with Stryker on Visualization in Spine Surgery
Synaptive Medical expanded its automation and robotics applications into spine, and entered into a co-marketing collaboration with Stryke...
First Cases with hipEOS 3.0 and Intellijoint HIP Smart Navigation
First patient cases have occurred using EOS Imaging's hipEOS 3.0 surgical planning software delivered by Intellijoint HIP®, Intellijoint S...
Stryker Completes Acquisition of Mobius Imaging/Cardan Robotics
Stryker completed its acquisition of Mobius Imaging and Cardan Robotics, specialists in point-of-care imaging....
7D Surgical Makes Milestone 30th Sale of Machine-vision Image Guided Technology
7D Surgical completed 30 sales since commercial launch of its Machine-vision Image Guided Surgery platform for spinal and cranial surgery.
Smith+Nephew CEO Stepping Down
Smith+Nephew CEO Namal Nawana will step down from his position on October 31, by mutual agreement, to pursue opportunities outside of the U.K.
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.
LimaCorporate to Distribute Dedienne Sante Dual Mobility Cups
LimaCorporate entered into an agreement with Dedienne Santé for distribution of the SYMBOL® dual mobility acetabular cup.
BioPoly Granted New U.S. Patent
BioPoly was granted an additional U.S. patent for its partial resurfacing implants.
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.
Episurf Medical Granted Patent Approval in the U.K.
Episurf Medical was issued an Intention to Grant for a patent addressing damage marking technology for use in knee repair.
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.
THINK Surgical Gains FDA Clearance for Robotic Knee Replacement Application
THINK Surgical received FDA 510(k) clearance to market the TSolution One® Total Knee Application for pre-surgical planning.
HD LifeSciences Announces Fluid Channels Patent Allowance
HD LifeSciences received a patent allowance notice addressing fluid channel technology employed in its interbody fusion devices. 
Medacta Gains CE Mark for Lateralized Glenosphere
Medacta received CE Mark approval for a lateralized glenosphere component, expanding its range of reverse shoulder replacement options.
Aegis Spine Gains FDA Clearance for AccelFix Expandable Cage
Aegis Spine received FDA 510(k) clearance to market the AccelFix Expandable Cage System.
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