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Humerus Articles & Analysis

14 news found

Daxor Corporation Appoints Linda Cooper, Vice President Project Management

Daxor Corporation Appoints Linda Cooper, Vice President Project Management

Daxor Corporation (Nasdaq: DXR), the global leader in blood volume measurement technology, today announces the appointment of Linda Cooper as Vice President of Project Management. “Linda joins Daxor with over 30 years of experience in product development and commercialization in the medical device industry. Linda’s proven track record makes her an excellent addition to the Daxor team ...

ByDaxor Corporation


Bonezone Features Shoulder Innovations

Bonezone Features Shoulder Innovations

The rocking horse effect occurs when the humerus both rotates and translates on the scapula as it articulates. ...

ByShoulder Innovations


Catalyst OrthoScience Features Innovative Products And Shoulder Surgery Leaders At AAOS

Catalyst OrthoScience Features Innovative Products And Shoulder Surgery Leaders At AAOS

Visit booth #2408 for product demonstrations of the Archer™ Shoulder Systems NAPLES, Fla., March 22, 2022 – Catalyst OrthoScience Inc. (Catalyst), a medical device company focused on the upper extremity orthopedics market, will be at the American Academy of Orthopedic Surgeons (AAOS) 2022 Annual Meeting, March 23-25, 2022, in Chicago. At booth #2408, Catalyst will have demos and the ...

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 already includes ...

ByShoulder Innovations


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

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

RSIP Vision’s new tool utilizes the shoulder MRI scan, without compromising on resolution quality. It automatically segments the humerus and scapula from the scan. The segmentation output goes through another neural network, trained to upgrade segmentation resolution, thus producing a super-resolution model despite the original scan limitations. ...

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

HOLLAND, Mich., August 23, 2021 — Shoulder Innovations Inc, a leading innovator in the development of shoulder replacement systems, announced today that they have received FDA clearance for their InSet™ Reverse Shoulder Arthroplasty System. The InSet™ Reverse Shoulder system seamlessly integrates and rounds out a best in class product line for shoulder arthroplasty including: ...

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

In the US, the IlluminOss System is now indicated for use in skeletally mature patients in the treatment of traumatic, fragility, pathological, and impending pathological fractures of the humerus, radius, ulna, clavicle, pelvis, fibula, metacarpals, metatarsals, and phalanges. ...

ByIlluminOss Medical, Inc.


IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

IlluminOss Medical Receives FDA Clearance for Use in Fibula Fractures

In the US, the IlluminOss System was previously cleared by the FDA for the treatment of traumatic, fragility, pathological, and impending pathological fractures of the humerus, radius, ulna, clavicle, pelvis, metacarpals, metatarsals, and phalanges. ...

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

In the US, the IlluminOss System was previously cleared by the FDA for the treatment of traumatic, fragility, pathological, and impending pathological fractures of the humerus, radius, and ulna. IlluminOss can be also used in conjunction with FDA-cleared fracture fixation systems to provide supplemental fixation in compromised bone in all cleared anatomic sites. ...

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.

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 FDA clearance for these exciting new indications*, having been previously available solely for the treatment of pathological and impending pathological fractures associated with metastatic disease in ...

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.

Food and Drug Administration (FDA) for use in skeletally mature patients in the treatment of traumatic, fragility, pathological, and impending pathological fractures of the humerus, radius and ulna. “IlluminOss’ minimally invasive approach isideal for treating patients suffering from fragility fractures. ...

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

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. The IlluminOss System incorporates the use of a thin-walled PET balloon that is infused with a liquid monomer and delivered in a minimally invasive fashion into ...

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’ LightFix Trial is a multi-center study of the IlluminOss System for the treatment of impending and actual pathological fractures in the humerus from metastatic bone disease Preliminary results from the U.S. trial measured pain and functional improvement, as well as evaluated safety and performance. ...

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

Thirteen surgical sites around the country participated in the trial, which included 80 patients - all with impending or pathologic fractures in the humerus due to metastatic carcinoma. IlluminOss’ minimally invasive procedure incorporates the use of a thin walled PET balloon that is infused with a liquid monomer and inserted into the intramedullary canal of the bone ...

ByIlluminOss Medical, Inc.

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