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Orthopedic Devices News

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151-165 of 1575 results
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
Acumed launches new system for ankle fractures
By MDBR Staff Writer
The Acumed Ankle Plating System 3 and Small Fragment Base Set features a variety of fracture-specific plating options designed to address fractures of the distal tibia and fibula. The system marks the company's continued commitment to provide industry-leading fracture fixation solutions.
Specialty Devices > Orthopedic Devices > News
Centinel Spine expands STALIF internationally
By MDBR Staff Writer
Centinel Spine, the pioneer of Stand-Alone, No-Profile®, Integrated Interbody™ fusion devices, expands its MIDLINE II-Ti product family, a Ti-ACTIVE™ coated, No-Profile, anterior lumbar Integrated Interbody device, in the United States and Australia.
Specialty Devices > Orthopedic Devices > News
Interventional Spine announces FDA clearance of Lordotic Opticage
By MDBR Staff Writer
Interventional Spine announced FDA clearance of its 80 Lumbar Lordotic Opticage Expandable Intervertebral Body Fusion Device.
Specialty Devices > Orthopedic Devices > News
Implanet’s new Jazz Claw hybrid implant gets FDA and CE mark approval
Medical technology company Implanet has secured the US Food and Drug Adminstration’s 510(k) clearance and CE mark approval for its new Jazz Claw hybrid implant.
Specialty Devices > Orthopedic Devices > News
Orthofix announces 510(k) clearance and US limited market launch of Forza PTC interbody spacer system
By MDBR Staff Writer
Orthofix International, a diversified, global medical device company, today announced the 510(k) clearance and U.S. limited market launch of the FORZA® PTC™ (Peek Titanium Composite) Spacer System.
Specialty Devices > Orthopedic Devices > News
First Ray’s CortiClamp small bone fixation system gets FDA approval
By MDBR Staff Writer
Medical device firm First Ray has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its CortiClamp system for small bone fixation.
Specialty Devices > Orthopedic Devices > News
151-165 of 1575 results