FDA Approves Hologics Less Invasive Permanent Contraception System

FDA has given final approval to Hologics Adiana permanent contraception system, the Boston Herald reports. The company hopes to market the procedure as an alternative to tubal ligation surgery for the roughly 700,000 U.S. women who undergo the procedure each year. Adiana is similar to Conceptus Essure, which has been on the market since 2002.

Adiana involves a twostep procedure that can be performed in about 15 minutes in a doctors office. The process consists of inserting a catheter into the fallopian tubes and delivering a low level of radio frequency energy to make a small lesion on the inside lining of each tube. The catheter then implants silicone polymer inserts, about the size of a grain of rice, on top of the lesions. The tubes become blocked as healthy cell tissue attaches to the inserts (McConville, Boston Herald, 7/9).

Reprinted with kind permission from nationalpartnership.org. You can view the entire Daily Womens Health Policy Report, search the archives, or sign up for email delivery here. The Daily Womens Health Policy Report is a free service of the National Partnership for Women & Families, published by The Advisory Board Company.

© 2009 The Advisory Board Company. All rights reserved.

This entry was posted on Lunes, Julio 13th, 2009 at 17:20 and is filed under sexual health. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.

Leave a Reply