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Biomaterials Implant Articles & Analysis

13 news found

RevBio Receives Approval from the U.K.’s Regulatory Authority to Initiate a Clinical Trial for an Optimized Formulation of its Dental Bone Adhesive Biomaterial

RevBio Receives Approval from the U.K.’s Regulatory Authority to Initiate a Clinical Trial for an Optimized Formulation of its Dental Bone Adhesive Biomaterial

RevBio, Inc., announced that it has received approval from the Medicines and Healthcare products Regulatory Agency in the United Kingdom to start a 15-patient clinical trial to examine the safety and efficacy of immediately stabilized dental implants following tooth extractions using an optimized formulation of Tetranite®, the company’s bone adhesive ...

ByRevBio Inc.


LaunchPad Medical Initiates its First European Clinical Study

LaunchPad Medical Initiates its First European Clinical Study

LaunchPad Medical, Inc. announced that it has received approval from the Medicines and Healthcare products Regulatory Agency in the United Kingdom to start a 15-patient pilot clinical study to examine the safety and efficacy of Tetranite, the company's bone adhesive biomaterial, to immediately stabilize dental implants following tooth extractions. ...

ByRevBio Inc.


Healionics’ Vascular Access Device Featured at American Society of Nephrology’s Kidney Week 2016

Healionics’ Vascular Access Device Featured at American Society of Nephrology’s Kidney Week 2016

Healionics’ STARport HD, a novel preclinical stage implantable device that allows needle-free bloodstream access for hemodialysis treatment, has been selected by the American Society of Nephrology (ASN) to be featured at the ASN exhibit booth at Kidney Week 2016 as one of several new technologies portraying the future of kidney disease treatment. ...

ByHealionics


Healionics Announces New CEO

Healionics Announces New CEO

” About Healionics Corporation Healionics develops and manufactures synthetic biomaterials and implantable medical devices that offer reduced foreign body reaction, fibrotic encapsulation and infection risk. The precisely controlled pore structure of Healionics’ innovative STAR® technology induces a favorable healing response and improves tissue ...

ByHealionics


Healionics Awarded $1.5M SBIR Grant from NIH to Advance Clot-Resistant Synthetic Vascular Graft for Dialysis Patients

Healionics Awarded $1.5M SBIR Grant from NIH to Advance Clot-Resistant Synthetic Vascular Graft for Dialysis Patients

” About Healionics Corporation Healionics develops and manufactures STAR Biomaterials for implanted medical devices. The precisely controlled pore structure of the innovative STAR technology induces a favorable integrated healing response, overcoming fibrotic reactions and infection issues to enhance medical device performance and longevity. ...

ByHealionics


Healionics Awarded SBIR Contract from DOD to Develop Biointegrated Synthetic Vascular Graft

Healionics Awarded SBIR Contract from DOD to Develop Biointegrated Synthetic Vascular Graft

About Healionics Corporation Healionics develops and manufactures STAR Biomaterials for implanted medical devices. The precisely controlled pore structure of the innovative STAR technology induces a favorable integrated healing response, overcoming fibrotic reactions and infection issues to enhance medical device performance and ...

ByHealionics


Healionics Receives SBIR Grant from National Institutes of Health to Develop Needle Free Dialysis Access Devices

Healionics Receives SBIR Grant from National Institutes of Health to Develop Needle Free Dialysis Access Devices

Titled, “Vascular Grafts for Needle Free Dialysis Access Devices,” the grant provides one-year funding to develop Healionics’ new STARgraft - a vascular graft based on STAR biomaterial that shows promise to reduce thrombosis and infection issues. ...

ByHealionics


Second Patent Issued for Healionics’ Textured STAR Biointerface

Second Patent Issued for Healionics’ Textured STAR Biointerface

The STAR Biointerface is a textured porous tissue ingrowth layer that enhances the biocompatibility and infection resistance of implanted medical devices. The ingrowth layer can be formed by adhering granules of a porous biomaterial to a device surface. ...

ByHealionics


ASTM F2042 - 00(2011) Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part II—Crosslinking and Fabrication

ASTM F2042 - 00(2011) Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part II—Crosslinking and Fabrication

Referenced Documents (purchase separately) ASTM Standards D395 Test Methods for Rubber Property--Compression Set D412 Test Methods for Vulcanized Rubber and Thermoplastic Elastomers--Tension D430 Test Methods for Rubber Deterioration--Dynamic Fatigue D624 Test Method for Tear Strength of Conventional Vulcanized Rubber and Thermoplastic Elastomers D792 Test Methods for Specific Gravity ...

ByASTM International


ASTM F755 - 99(2011) Standard Specification for Selection of Porous Polyethylene for Use in Surgical Implants

ASTM F755 - 99(2011) Standard Specification for Selection of Porous Polyethylene for Use in Surgical Implants

This specification covers the raw material and final product requirements, and the associated test methods for the selection of porous high density and ultra high molecular weight polyethylenes intended for use in surgical implants. The porous polyethylene may be used as a free standing product or as a coating on a substrate in ...

ByASTM International


ASTM F136 - 11 Standard Specification for Wrought Titanium-6Aluminum-4Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications (UNS R56401)

ASTM F136 - 11 Standard Specification for Wrought Titanium-6Aluminum-4Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications (UNS R56401)

This specification covers the chemical, mechanical, and metallurgical requirements for wrought annealed titanium-6aluminum-4vanadium ELI (extra low interstitial) alloy (R56401) to be used in the manufacture of surgical implants. The products are classified into: strip, sheet, plate, bar, forging bar, and wire. ...

ByASTM International


ASTM F2083 - 11 Standard Specification for Total Knee Prosthesis

ASTM F2083 - 11 Standard Specification for Total Knee Prosthesis

Referenced Documents (purchase separately) ASTM Standards F67 Specification for Unalloyed Titanium, for Surgical Implant Applications (UNS R50250, UNS R50400, UNS R50550, UNS R50700) F75 Specification for Cobalt-28 Chromium-6 Molybdenum Alloy Castings and Casting Alloy for Surgical Implants (UNS R30075) F86 Practice for Surface Preparation and Marking of ...

ByASTM International


ASTM F2066 - 11 standard specification for wrought titanium-15 molybdenum alloy for surgical implant applications (UNS R58150)

ASTM F2066 - 11 standard specification for wrought titanium-15 molybdenum alloy for surgical implant applications (UNS R58150)

This specification covers the chemical, mechanical, and metallurgical requirements for wrought titanium-15 molybdenum alloy to be used in the manufacture of surgical implants. The product shall be classified as: strip; ...

ByASTM International

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