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Humeral Articles & Analysis

14 news found

Daxor Corporation Appoints Linda Cooper, Vice President Project Management

Daxor Corporation Appoints Linda Cooper, Vice President Project Management

She earned her Bachelor of Science degree in biomedical engineering from the University of Iowa and is an inventor on a U.S. patent for a bone plate system for repair of proximal humeral fracture. “It is an exciting time to be joining Daxor as we prepare to submit our next generation systems in preparation for the most important technology launch for the company in twenty ...

ByDaxor Corporation


Bonezone Features Shoulder Innovations

Bonezone Features Shoulder Innovations

“We used to have to worry about what size glenoid went with what size humeral head. Now, it doesn’t matter what size head you use with what size glenoid. ...

ByShoulder Innovations


Catalyst OrthoScience Features Innovative Products And Shoulder Surgery Leaders At AAOS

Catalyst OrthoScience Features Innovative Products And Shoulder Surgery Leaders At AAOS

At the Catalyst booth, attendees can experience the Catalyst Clinical Series featuring: “Subscapularis-Sparing Approach To Perform Anatomic TSA Using A Multiplanar Humeral Osteotomy And Angled Glenoid Instruments” presented by Steven Goldberg, MD of Physicians Regional Medical Group on Wednesday, March 23 from 1:00 - 1:30 pm CT “Improved Range of Motion ...

ByCatalyst OrthoScience Inc.


Shoulder Innovations Announces FDA Clearance of New InSet Stemless Humeral Implant

Shoulder Innovations Announces FDA Clearance of New InSet Stemless Humeral Implant

GRAND RAPIDS, Mich., March 14, 2022—Shoulder Innovations LLC., (SI), a leading innovator in the development of shoulder replacement systems, announces the FDA Clearance of their latest component of the InSetTM Total Shoulder System, the InSetTM Stemless Humeral System. The InSetTM Stemless implant is the latest addition to the innovative and integrated InSetTM system, which ...

ByShoulder Innovations


Announcement – Total Shoulder Arthroplasty (TSA) Planning Through MRI Scan

Announcement – Total Shoulder Arthroplasty (TSA) Planning Through MRI Scan

RSIP Vision, an experienced leader in driving innovation for medical imaging through advanced AI and computer vision solutions, today announces a new tool for Total Shoulder Arthroplasty (TSA) planning. This tool performs segmentation of the shoulder bones from shoulder MRI scan, which is usually performed in shoulder healthcare. The segmentation output undergoes super-resolution enhancement to ...

ByRSIP Vision


Shoulder Innovations Announces FDA 510(K) Clearance for InSet Reverse Shoulder Platform Technology

Shoulder Innovations Announces FDA 510(K) Clearance for InSet Reverse Shoulder Platform Technology

Broad range of implant types representing 6 different products, seamlessly integrated into one instrument tray allowing efficient treatment of patients with the simplest to the most complex pathologies, optimized for ASC environments, Convertible humeral platform demonstrating best in class fixation, the only true fully convertible humeral inlay system, and ...

ByShoulder Innovations


IlluminOss Medical Receives FDA Clearance for Use in Femur and Tibia Fractures as a Supplement to Approved Hardware

IlluminOss Medical Receives FDA Clearance for Use in Femur and Tibia Fractures as a Supplement to Approved Hardware

IlluminOss Medical, a medical device company focused on minimally invasive orthopedic fracture repair, today announced an expanded U.S. Food and Drug Administration (FDA 510k) clearance for its Photodynamic Bone Stabilization System. The new clearance allows IlluminOss to be used in femur and tibia fractures as supplemental fixation to FDA-cleared fracture fixation systems. “Femur and ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

IlluminOss Medical, a medical device company focused on minimally invasive orthopedic fracture repair, today announced that it has received expanded U.S. Food and Drug Administration (FDA 510k) clearance for its Photodynamic Bone Stabilization System for treatment of fractures of the fibula. The IlluminOss System is a minimally invasive approach for fracture repair and stabilization through a ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Receives FDA Clearance for Expanded Clinical Use for Pelvic, Clavicle and Small-Bone Fractures

IlluminOss Medical Receives FDA Clearance for Expanded Clinical Use for Pelvic, Clavicle and Small-Bone Fractures

IlluminOss Medical, a medical device company focused on minimally invasive orthopedic fracture repair, today announced that it has received expanded U.S. Food and Drug Administration (FDA 510k) clearance for its Photodynamic Bone Stabilization System for treatment of fractures of the pelvis, clavicle, and the small bones of the hands and feet: metacarpals, metatarsals, and phalanges. The ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Launches the IlluminOss Bone Stabilization System for Use in the Treatment of Traumatic and Fragility Fractures in the U.S.

IlluminOss Medical Launches the IlluminOss Bone Stabilization System for Use in the Treatment of Traumatic and Fragility Fractures in the U.S.

IlluminOss Medical, Inc., a privately held, commercialstage medical device company focused on minimally invasive orthopedic fracture repair, today announced the U.S. launch and commercial availability of the IlluminOss? Bone Stabilization System for use in skeletally mature patients in the treatment of traumatic and fragility fractures of the humerus, radius and ulna. IlluminOss recently obtained ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Receives Clearance to Expand Clinical Indications in the U.S.

IlluminOss Medical Receives Clearance to Expand Clinical Indications in the U.S.

IlluminOss Medical, a privately held, commercial-stage medical device company focused on minimally invasive orthopedic fracture repair, today announced that the IlluminOss Photodynamic Bone Stabilization System has received additional clinical clearance and is now indicated by the U.S. Food and Drug Administration (FDA) for use in skeletally mature patients in the treatment of traumatic, ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Granted FDA Marketing Clearance for the IlluminOss Bone Stabilization System

IlluminOss Medical Granted FDA Marketing Clearance for the IlluminOss Bone Stabilization System

IlluminOss Medical, a privately held, commercial-stage medical device company focused on minimally invasive orthopedic fracture repair, today announced that it has received U.S. Food and Drug Administration (FDA) de novo clearance for the IlluminOss Bone Stabilization System for treatment of impending and actual pathological fractures of the humerus, radius and ulna from metastatic bone disease. ...

ByIlluminOss Medical, Inc.


Preliminary Data Presented from First U.S. Clinical Trial of IlluminOss Medical`s Photodynamic Bone Stabilization System

Preliminary Data Presented from First U.S. Clinical Trial of IlluminOss Medical`s Photodynamic Bone Stabilization System

IlluminOss Medical, a privately-held, commercial stage medical device company focused on minimally invasive orthopedic fracture repair, today announced that Richard Terek, M.D., presented the first preliminary data from its U.S. pivotal clinical trial at the recent Musculoskeletal Tumor Society (MSTS) Meeting in Detroit. The IlluminOss System is the world’s only system of its kind which ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Completes Enrollment for U.S. Clinical Trial Using Groundbreaking Photodynamic Bone Stabilization System

IlluminOss Medical Completes Enrollment for U.S. Clinical Trial Using Groundbreaking Photodynamic Bone Stabilization System

“We’ve seen that the IlluminOss implant can be a game changer for patients with humeral metastatic disease. This technology allows us to stabilize the bone with less pain, less surgical time, and less difficulty for the patients. ...

ByIlluminOss Medical, Inc.

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