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FDA Advisory Panel Finds Hologic's Adiana(R) Permanent Contraception Approvable
Date:12/13/2007

ure approval by the FDA of the premarket application for Adiana Permanent Contraception for female sterilization and the benefits realizable by using the Adiana Permanent Contraception procedure. The Company cannot assure when or if FDA approval will be granted or that the anticipated efficacy of the Adiana Permanent Contraception procedure will be realizable. Factors that could adversely affect Hologic'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 any such statements to reflect any change in the Company's expectations or any change in events, conditions or circumstances on which any such statement is based.

(1) Westhoff C, Davis A. Tubal sterilization: focus on the U.S.

experience. Fertil Steril. 2000;73(5):913-922.

Editorial Contacts:

Jane Hauser or Sarah Belkner

Schwartz Communications

781-684-0770

Adiana@schwartz-pr.com

Hologic Contacts:

Frances Crecco

Director, Investor Relations

781-999-7377

Jeff Keene

Healthcare Media

508-263-8957


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SOURCE Hologic, Inc.
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