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FDA Approves Hologic's Makena™ (Formerly Referred to as Gestiva™) Pharmaceutical
Date:2/4/2011

h risk assessment, mini C-arm for extremity imaging and molecular diagnostic products including HPV and reagents for a variety of DNA and RNA analysis applications. For more information, visit www.hologic.com.

Hologic, Gestiva, Makena, and associated logos are trademarks and/or registered trademarks of Hologic, Inc. and/or its subsidiaries in the United States and/or other countries.

Forward Looking DisclaimerThis News Release contains forward-looking information that involves known and unknown risks and uncertainties. The Company cannot assure that KV will have the necessary cash funding available to make payments under this Agreement as they come due. The risks and uncertainties included above are not exhaustive. Other factors that could adversely affect the Company's business and prospects are described in the Company's filings with the Securities and Exchange Commission. Hologic expressly disclaims any obligation or undertaking to release publicly any updates or revisions to the data or statements presented herein to reflect any change in the Company's expectations or any change in events, conditions or circumstances on which any such data or statements are based. Contact:  

Deborah GordonVice President, Investor RelationsHologic, Inc.Deborah.gordon@hologic.com(781) 999-7716
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SOURCE Hologic, Inc.
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