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Orthopedic Devices News

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121-135 of 1566 results
Spinal Simplicity introduces innovative implant with hydroxyapatite coating
Spinal Simplicity, a medical device company based in Overland Park, Kan., that develops innovative solutions to treat complex surgical problems, recently announced a new generation of their Minuteman G3 fusion device that features an FDA-cleared coating of hydroxyapatite (HA).
Specialty Devices > Orthopedic Devices > News
Titan Spine expands distribution deal with MBA to offer Endoskeleton titanium implant portfolio in Italy
Titan Spine, a medical device surface technology company focused on developing innovative spinal interbody fusion implants, today announced that it has expanded its distribution agreement with strategic partner MBA to provide Titan’s line of Endoskeleton titanium implants to practicing spine surgeons in the European Union to include Italy.
Specialty Devices > Orthopedic Devices > News
DT MedTech’s Hintermann Series H3 lower extremity medical devices win CE mark approval
By MDBR Staff Writer
DT MedTech (DTMT) has received CE mark approval for the Hintermann Series H3 total ankle replacement devices.
Specialty Devices > Orthopedic Devices > News
FDA approves Centric Medical’s Hammertoe correction system
By MDBR Staff Writer
Centric Medical has received 510(k) clearance from the US Food and Drug Administration (FDA) for its Hammertoe correction system.
Specialty Devices > Orthopedic Devices > News
BONESUPPORT receives FDA approval to initiate IDE clinical study
BONESUPPORT AB, an emerging leader in innovative injectable bioceramic bone substitute products to treat bone voids caused by trauma, infection, disease or related surgery, announced that it has received approval from the US Food and Drug Administration (FDA) to begin an IDE (Investigational Device Exemption) study with CERAMENT G.
Specialty Devices > Orthopedic Devices > News
Orthopaedic Implant Company introduces new intramedullary femur nail system
By MDBR Staff Writer
The Orthopaedic Implant Company (OIC) has introduced new intramedullary femur nail system to treat femoral midshaft and distal fractures.
Specialty Devices > Orthopedic Devices > News
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
121-135 of 1566 results