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Orthopedic Devices News

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136-150 of 1575 results
Essential Medical gets FDA approval to begin US clinical trial for X-Seal 6F vascular closure device
Essential Medical, a privately held medical device company addressing the vascular closure market, announced that it has received Investigational Device Exemption (IDE) approval from the FDA to begin the U.S. clinical trial for X-Seal, the company's 6F Vascular Closure Device.
Specialty Devices > Orthopedic Devices > News
Gore’s Tigris vascular stent gets FDA approval to treat peripheral artery disease
By MDBR Staff Writer
W. L. Gore & Associates has received approval from the US Food and Drug Administration (FDA) for its Tigris dual-component vascular stent to treat peripheral artery disease (PAD).
Specialty Devices > Orthopedic Devices > News
Orthofix wins Japanese approval for Phoenix minimally invasive spinal fixation system
By MDBR Staff Writer
Medical device firm Orthofix International has secured approval from the Japanese Ministry of Health, Labor and Welfare (MHLW) for its Phoenix minimally invasive spinal (MIS) fixation system.
Specialty Devices > Orthopedic Devices > News
4WEB Medical gets FDA approval for lateral interbody fusion device
By MDBR Staff Writer
Implant device company 4WEB Medical has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its Lateral Spine truss system.
Specialty Devices > Orthopedic Devices > News
Medtronic launches new VariLoc system to treat fractures
By MDBR Staff Writer
Irish medical technology firm Medtronic has introduced VariLoc locking compression plate system in China and other select countries.
Specialty Devices > Orthopedic Devices > News
Globus Medical to acquire Alphatec’s international business for $80m
By MDBR Staff Writer
Globus Medical has signed an agreement to acquire Alphatec Holdings' international operations and distribution channels for $80m.
Specialty Devices > Orthopedic Devices > News
Relievant Medsystems’ Intracept system gets FDA approval to treat chronic low back pain
By MDBR Staff Writer
Medical device firm Relievant Medsystems has secured 510(k) clearance from the US Food and Drug Administration for its Intracept intraosseous nerve ablation system.
Specialty Devices > Orthopedic Devices > News
Medtronic launches revamped minimally invasive spine fusion procedures
Medtronic announced the continued development of the OLIF Platform with the launch of the Pivox Oblique Lateral Spinal System with Lateral Plate for OLIF25 and Divergence-L Anterior/Oblique Lumbar Fusion System for OLIF51 at the International Meeting on Advanced Spine Techniques (IMAST) in Washington, D.C.
Specialty Devices > Orthopedic Devices > News
Active Ankle debuts newly engineered ankle braces
Active Ankle debuts the Eclipse II and Eclipse I, two best-in-class multi-sport rigid ankle braces with improved durability, design, comfort and mobility. c
Specialty Devices > Orthopedic Devices > News
ulrich medical USA introduces new neon3 posterior cervical system
By MDBR Staff Writer
Medical device firm ulrich medical USA has expanded its cervical spinal implant portfolio with the introduction of new neon3 posterior cervical system.
Specialty Devices > Orthopedic Devices > News
Mobius Bionics to launch Luke prosthetic arm later this year
By MDBR Staff Writer
Medical device firm Mobius Bionics is set launch its new Luke prosthetic arm later this year.
Specialty Devices > Orthopedic Devices > News
DonJoy Performance introduces POD ankle brace
By MDBR Staff Writer
DonJoy Performance, the consumer division of leading global provider of medical device solutions for musculoskeletal health, vascular health and pain management, DJO Global, Inc., today announced the product introduction of the Protection On Demand Ankle Brace (POD).
Specialty Devices > Orthopedic Devices > News
Cartiva gets FDA premarket approval for Cartiva synthetic cartilage implant
By MDBR Staff Writer
Cartiva, a developer of innovative products for the treatment of cartilage damage and osteoarthritis, announced that it received Premarket Approval (PMA) from the U.S. Food and Drug Administration (FDA) for its Cartiva Synthetic Cartilage Implant (SCI) for arthritis of the big toe joint.
Specialty Devices > Orthopedic Devices > News
Centric Medical gets 510(k) clearance for Subtalar arthroereisis implant system for foot and ankle
By MDBR Staff Writer
Centric Medical, a division of Life Spine, announced that the US Food and Drug Administration (FDA) has given 510(k) marketing clearance to the Subtalar Arthroereisis Implant System for treating hyperpronation of the foot and stabilization of the subtalar joint.
Specialty Devices > Orthopedic Devices > News
University of Bristol scientists develop new bio-ink for 3D printing of complex tissues
By MDBR Staff Writer
Researchers from the University of Bristol have developed a new bio-ink to enable the production of complex tissues for surgical implants.
Specialty Devices > Orthopedic Devices > News
136-150 of 1575 results