AbbeyMoor Medical, Inc

www.abbeymoormedical.com

AbbeyMoor Medical’s mission is to improve patient quality of life and enhance healthcare delivery through the development of innovative medical devices and procedures. This will be accomplished by applying the latest technologies to develop safe and effective healthcare products that are minimally invasive and cost effective. Privately held, AbbeyMoor has been the recipient of angel-funding since its inception. And conducting good science has been its goal. Currently holding 13 U.S. patents, with 8 under review, and 12 patents pending internationally, intellectual property is the cornerstone of The Company. Their first product, The Spanner™ temporary stent for the prostate, is designed for men with urinary voiding dysfunction due to an obstructed prostate. The Spanner™Prostatic Stent has received CE Mark and FDA approval and is currently marketed in the U.S. and abroad. The American Medical Association (AMA) has established Category I CPT®* code 53855 for the insertion of a temporary urethral stent for the prostate, including urethral measurement. The Spanner stent has been designed to open the prostatic urethra and allow patients to maintain urine flow and experience volitional voiding by reducing urethral resistance within the prostate. The Spanner stent is an alternative for some patients** to indwelling Foley catheterization, clean intermittent catheterization, or a suprapubic tube.

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AbbeyMoor Medical’s mission is to improve patient quality of life and enhance healthcare delivery through the development of innovative medical devices and procedures. This will be accomplished by applying the latest technologies to develop safe and effective healthcare products that are minimally invasive and cost effective. Privately held, AbbeyMoor has been the recipient of angel-funding since its inception. And conducting good science has been its goal. Currently holding 13 U.S. patents, with 8 under review, and 12 patents pending internationally, intellectual property is the cornerstone of The Company. Their first product, The Spanner™ temporary stent for the prostate, is designed for men with urinary voiding dysfunction due to an obstructed prostate. The Spanner™Prostatic Stent has received CE Mark and FDA approval and is currently marketed in the U.S. and abroad. The American Medical Association (AMA) has established Category I CPT®* code 53855 for the insertion of a temporary urethral stent for the prostate, including urethral measurement. The Spanner stent has been designed to open the prostatic urethra and allow patients to maintain urine flow and experience volitional voiding by reducing urethral resistance within the prostate. The Spanner stent is an alternative for some patients** to indwelling Foley catheterization, clean intermittent catheterization, or a suprapubic tube.

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Country

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State

Minnesota

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Employees

11-50

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Founded

1996

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Estimated Revenue

$1,000,000 to $5,000,000

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Social

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Potential Decision Makers

  • Co - Founder , Chief Executive Officer , and Chairman

    Email ****** @****.com
    Phone (***) ****-****
  • Chief Executive Officer and President

    Email ****** @****.com
    Phone (***) ****-****

Technologies

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