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November 27, 2015 4:31 AM ET

Healthcare Equipment and Supplies

Company Overview of Progyny, Inc.

Company Overview

Progyny, Inc. offers women’s reproductive health by translating scientific discoveries into clinical solutions that are aimed at improving patient outcomes. It offers Eeva Test that is used adjunctively to traditional morphology and provides in vitro fertilization clinicians and patients with objective information about embryo development potential to aid in embryo selection. Progyny, Inc. was formerly known as Auxogyn, Inc. and changed its name to Progyny, Inc. in April, 2015. The company was incorporated in 2008 and is based in Menlo Park, California.

1490 O’Brien Drive

Suite A

Menlo Park, CA 94025

United States

Founded in 2008





Key Executives for Progyny, Inc.

Chief Executive Officer and Director
President and Chief Operating Officer
Age: 49
Group Senior Vice President of Commercial Development
Vice President of Medical and Scientific Affairs
Vice President of Commercial Development
Compensation as of Fiscal Year 2015.

Progyny, Inc. Key Developments

Progyny Appoints Gary Hartonas as Senior Vice President, Commercial Development

Gary Harton, PhD has been appointed as new Group Senior Vice President, Commercial Development by Progyny. Dr. Harton would be playing the role for Progyny's commercial operations, comprising sales, marketing, and customer service operations throughout the products of Fertility, EggBanxx, IVFAdvantage and The Eeva Test, the first and only FDA-cleared test to use time lapse imaging combined with their proprietary algorithm to aid in embryo selection during IVF. Prior to joining, Dr. Harton had a long career in the area of Reproductive Sciences, comprising both laboratory management and IVF practice management posts.

Auxogyn, Inc. Presents at Wedbush 2014 Life Sciences Management Access Conference, Aug-12-2014 09:10 AM

Auxogyn, Inc. Presents at Wedbush 2014 Life Sciences Management Access Conference, Aug-12-2014 09:10 AM. Venue: Le Parker Meridien, New York, New York, United States.

Auxogyn, Inc. Receives FDA Clearance for its Eeva(TM) System

Auxogyn, Inc. announced that its first product, the Eeva System, received clearance from the U.S. Food and Drug Administration through its de novo classification process, a regulatory pathway for select novel, low- to moderate-risk medical devices that are first-of-a-kind. The Eeva System enables in vitro fertilization (IVF) clinicians to offer the proprietary Eeva Test, which is the first prognostic, non-invasive test that provides objective information regarding embryo development to help optimize treatment plans for their patients.

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