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Orthopedic Devices News

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46-60 of 1575 results
FDA approves CyMedica’s app-controlled muscle activation therapy
By MDBR Staff Writer
CyMedica Orthopedics has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its e-vive app-controlled and data-driven muscle activation therapy and patient engagement solution.
Specialty Devices > Orthopedic Devices > News
FDA approves SpineGuard's DSG integration module to make pedicle screws smart
By MDBR Staff Writer
SpineGuard has secured approval from the US Food and Drug Administration (FDA) for its new DSG (dynamic surgical guidance) integration module for making pedicle screws smart.
Specialty Devices > Orthopedic Devices > News
Safe Orthopaedics launches Walnut cervical cage bone substitute in Europe
By MDBR Staff Writer
French medical technology Safe Orthopaedics has introduced a bone substitute for its Walnut cervical cage in Europe.
Specialty Devices > Orthopedic Devices > News
Orthocell announces collaboration with Johnson & Johnson Innovation
Regenerative medicine company Orthocell has announced a research collaboration agreement with DePuy Synthes Products, part of the Johnson & Johnson Family of Companies, for its Ortho-ATI stem cell approach for the regeneration of degenerate tendons and ligaments.
Specialty Devices > Orthopedic Devices > News
Osseon receives new patent for steerable and curvable cavity creation system
Osseon has received a new patent for a steerable and curvable cavity creation system, with number US 9,510,885.
Specialty Devices > Orthopedic Devices > News
Medovex signs international distribution agreement with AlfaMed
Medovex, a developer of medical technology products, has entered into an international distribution agreement with AlfaMed, a supplier of innovative spine surgery equipment.
Specialty Devices > Orthopedic Devices > News
Medicrea announces 510(k) submission for FDA clearance of 3D-printed titanium spinal interbody devices
The Medicrea Group has announced the filing of its 510(k) submission to the US Food and Drug Administration (FDA) for approval of the company’s 3D-printed Titanium interbody devices, with compatible UNiD Lab personalized surgical planning and analytical services.
Specialty Devices > Orthopedic Devices > News
AVEX raises $7.6m in series A financing round to support launch of Footbeat
AVEX announced the securing of $7.6m in series A financing that will fuel the Q1 2017 launch of Footbeat.
Specialty Devices > Orthopedic Devices > News
Johnson & Johnson Medical Devices Companies introduce Orthopaedic Episode of Care Approach
The Johnson & Johnson Medical Devices Companies announced their Orthopaedic Episode of Care Approach, a comprehensive offering under their CareAdvantage capabilities, designed to help health systems and surgeons reduce costs and increase quality to drive improvements in orthopaedic care and achieve the goals of value-based alternative care models.
Specialty Devices > Orthopedic Devices > News
Orthofix’s new bone growth stimulators get CE mark and FDA approval
By MDBR Staff Writer
Orthofix International has secured the US Food and Drug Administration (FDA) clearance and CE mark approval for its next-generation CervicalStim and SpinalStim bone growth stimulators.
Specialty Devices > Orthopedic Devices > News
Globus Medical gets CE mark for Excelsius GPS guidance and navigation system
By MDBR Staff Writer
Musculoskeletal implant manufacturer Globus Medical has secured CE mark approval for Excelsius GPS robotic trajectory guidance and navigation system.
Specialty Devices > Orthopedic Devices > News
DePuy Synthes buys Interventional Spine’s expandable cage technology
By MDBR Staff Writer
Johnson & Johnson’s unit DePuy Synthes Products has signed an asset purchase and development agreement with Interventional Spine, which produces expandable cage and minimally invasive surgery (MIS) technologies for spinal fusion.
Specialty Devices > Orthopedic Devices > News
FDA approves CartiHeal's IDE application for Agili-C implant to treat joint surface lesions
By MDBR Staff Writer
The US Food and Drug Administration (FDA) has approved CartiHeal's investigational device exemption (IDE) application for Agili-C implant to treat joint surface lesions.
Specialty Devices > Orthopedic Devices > News
Allergan to buy Acelity’s LifeCell business unit for $2.9bn
By MDBR Staff Writer
Drugmaker Allergan has agreed to acquire LifeCell, a regenerative medicine unit owned by privately held medical device firm Acelity, for $2.9bn.
Specialty Devices > Orthopedic Devices > News
Meyers & Flowers Law Firm announces new settlement agreement with Stryker
The Multidistrict Litigation (MDL) Plaintiffs’ lead counsel committee, chaired by Peter J. Flowers of Meyers & Flowers, a Chicago-based law firm, reached a new settlement agreement for numerous patients involved in on-going litigation against Stryker and Howmedica Osteonics for complications involving the defective Stryker Modular Rejuvenate and ABG II Femoral Hip Implants.
Specialty Devices > Orthopedic Devices > News
46-60 of 1575 results