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Orthopedic Devices News

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136-150 of 1566 results
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
Centinel Spine completes successful evaluation of STALIF L
By MDBR Staff Writer
Centinel Spine, the pioneer of the No-Profile, Integrated Interbody fusion device market, completes Alpha release of STALIF L™ No-Profile, lateral lumbar Integrated Interbody device cleared by the U.S. Food and Drug Administration (FDA).
Specialty Devices > Orthopedic Devices > News
Exactech launches Acapella One cervical spacer system
By MDBR Staff Writer
Exactech, a developer and producer of bone and joint restoration products and biologic materials for extremities, knee, hip and spine, announced the full launch of the new Acapella One cervical spacer system.
Specialty Devices > Orthopedic Devices > News
Spineology expands its line of interbody devices
Spineology continues its focus on anatomy-conserving surgery with release of the Elite Expandable Interbody Fusion System.
Specialty Devices > Orthopedic Devices > News
SpineGuard receives US FDA clearance to market PediGuard threaded DSG device
By MDBR Staff Writer
SpineGuard, an innovative company that develops and markets disposable medical devices that empower surgeons to enhance clinical outcomes and simplify surgeries, announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its new PediGuard Threaded DSG™ device.
Specialty Devices > Orthopedic Devices > News
Tyber Medical expands FDA 510(k) clearance of headed and snap-off screws
By MDBR Staff Writer
Tyber Medical, a company focused on providing rapid private label commercialization with innovative orthopedic and spine devices including bioengineered surfaces, announces FDA 510K clearance of their headed and snap-off screws systems.
Specialty Devices > Orthopedic Devices > News
SI-BONE gets 510(k) clearance for updated indication for iFuse implant system
By MDBR Staff Writer
SI-BONE, a medical device company that pioneered the use of the iFuse Implant System® ("iFuse"), a minimally invasive surgical (MIS) device indicated for fusion for certain disorders of the sacroiliac (SI) joint, announced that the U.S. Food and Drug Administration (FDA) has cleared a 510(k) to allow modification of its indication statement noting that clinical studies have demonstrated that treatment with the iFuse Implant System improve pain, patient function and quality of life.
Specialty Devices > Orthopedic Devices > News
Zimmer Biomet to buy medical device firm LDR for $1bn
By MDBR Staff Writer
Zimmer Biomet Holdings has signed an agreement to acquire medical device firm LDR Holding for about $1bn.
Specialty Devices > Orthopedic Devices > News
First Ray’s SpeedButton soft tissue attachment system wins FDA approval
By MDBR Staff Writer
Medical device firm First Ray has secured 510(k) clearance from the US Food and Drug Adminsitration (FDA) for its SpeedButton system to attach soft tissue to bone.
Specialty Devices > Orthopedic Devices > News
Tyber Medical enters Australian market
By MDBR Staff Writer
Tyber Medical, a privately held medical device company focused on developing innovative orthopaedic and spine devices for private label opportunities, announces the acceptance of its entire interbody family of products into the Australian Registry of Therapeutic Goods.
Specialty Devices > Orthopedic Devices > News
136-150 of 1566 results