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March 26, 2015 3:31 PM ET

Healthcare Equipment and Supplies

Company Overview of ConforMIS, Inc.

Company Overview

ConforMIS, Inc., a medical device company, designs, develops, manufactures, and commercializes customized orthopedic implants and instrumentation in the United States. It offers femoral and tibial knee implants for the treatment of osteoarthritis and joint damages. The company was founded in 2004 and is based in Bedford, Massachusetts.

28 Crosby Drive

Bedford, MA 01730

United States

Founded in 2004

Phone:

781-345-9001

Fax:

781-345-0147

Key Executives for ConforMIS, Inc.

Founder, Chairman, Chief Executive Officer and President
Chief Financial Officer
Age: 50
Senior Vice President of Operations
Chief Legal Officer and General Counsel
Senior Vice President of Knee Implant Engineering
Compensation as of Fiscal Year 2014.

ConforMIS, Inc. Key Developments

ConforMIS, Inc. Presents at 33rd Annual J.P. Morgan Healthcare Conference, Jan-14-2015 04:00 PM

ConforMIS, Inc. Presents at 33rd Annual J.P. Morgan Healthcare Conference, Jan-14-2015 04:00 PM. Venue: Westin St. Francis Hotel, San Francisco, California, United States. Speakers: Philipp Lang, Founder, Chairman, Chief Executive Officer and President.

Bonutti Skeletal Innovations LLC Enters into Settlement and Patent License Agreement with ConforMIS, Inc

Acacia Research Corporation announced that Bonutti Skeletal Innovations LLC has entered into a settlement and patent license agreement with ConforMIS, Inc. The agreement resolves all aspects of the litigation for the United States District Court for the District of Delaware and the United States District Court for the District of Massachusetts.

Perdue & Kidd Files First Suit against ConforMIS, Inc. for Defective Custom Knee Implants

Perdue & Kidd filed a lawsuit against ConforMIS, Inc. this week, claiming the ConforMIS iTotal G2 custom knees were defective and injured plaintiff, Mary Jane Martine. This is the first lawsuit filed in the country against ConforMIS with these allegations. Mary Jane Martine, a 65-year-old nurse, had two separate knee replacement surgeries with the ConforMIS iTotal G2 knee, the first in October 2012 and the second in April 2013. By December 2013, Mary Jane began experiencing a host of complications with her right knee replacement. She suffered from severe knee pain, heard popping sounds, and was unable to extend her knee or even stand on it. Mary Jane's doctor found that both her right and left iTotal G2 implants were defective. Mary Jane was left with no option but to undergo bilateral implant removal surgery because both of her ConforMIS knees were not working and could not be salvaged. The ConforMIS iTotal G2 knee replacement line was cleared by the US Food and Drug Administration (FDA) through the 510(k) process in September 2012. While ConforMIS claimed to the FDA that its iTotal G2 knee was substantially similar to devices previously cleared for sale, it marketed the implants as a new and different design for knee replacement.

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