Healthcare Industry News:  Dermal Filler 

Devices

 News Release - February 7, 2007

Artes Medical Announces Commercial Launch of ArteFill(R)

Initial Shipments of First and Only FDA-Approved Non-Resorbable Dermal Filler

SAN DIEGO--(HSMN NewsFeed)--Artes Medical, Inc. (Nasdaq: ARTE ), a medical technology company focused on developing, manufacturing and commercializing a new category of aesthetic injectable products for men and women, today announced its first shipment of ArteFill® to trained physicians. ArteFill is the first and only non-resorbable injectable filler for the correction of wrinkles known as smile lines or nasolabial folds, and was approved by the FDA in October 2006. Artes Medical established a direct sales organization and has trained the initial group of physicians on appropriate usage and injection techniques.

"We are excited to announce the availability of the first non-resorbable Dermal Filler to physicians and patients across the country," said Diane S. Goostree, President and Chief Executive Officer. "We believe ArteFill meets the needs of patients seeking long-lasting wrinkle correction and relief from the 'credit card fatigue' and 'injection fatigue' that may occur with temporary Dermal Fillers."

About ArteFill®

ArteFill is the first and only FDA-approved non-resorbable injectable Dermal Filler for the correction of wrinkles known as smile lines or nasolabial folds. The unique microspheres in ArteFill are not absorbed by the body and therefore provide the first-of-its-kind permanent support for long-lasting wrinkle correction in one to two treatments.

ArteFill was approved by the FDA in October 2006 based on data from the Company's 12-month controlled, randomized, double-masked, multi-center U.S. clinical trial, which compared outcomes for patients treated with ArteFill with those of patients treated with the leading bovine collagen-based filler. At the 6-month evaluation, which was the primary efficacy evaluation period for the clinical trial, the wrinkle correction in patients treated with ArteFill persisted and showed statistically significant improvement compared to the wrinkle correction in the patients treated with the collagen control, who returned to their pretreatment status. The ArteFill patients were also evaluated one year after treatment, demonstrating continued safety and wrinkle correction.

The Company recently completed a 5-year follow-up study of 145 patients who were treated with ArteFill in the Company's U.S. clinical trial. In addition to demonstrating the safety profile of ArteFill, the study showed statistically significant (pless than0.001) improvement in patient wrinkle correction five years after the patient's last ArteFill treatment, and a statistically significant (pless than0.002) improvement in wrinkle correction at the 5-year point compared to the 6-month evaluation period. As part of the study, physician investigators and patients were asked to provide their assessment of ArteFill treatment. Over 90% of the physician assessments were either "completely successful" or "very successful;" and over 90% of the patient assessments were either "very satisfied" or "satisfied." The Company intends to submit the data from the study to the FDA for review in order to enhance the product labeling for ArteFill.

About Artes Medical, Inc.

Artes Medical is a medical technology company focused on developing, manufacturing and commercializing a new category of aesthetic injectable products for the dermatology and plastic surgery markets. The Company's initial product, ArteFill®, is being marketed to men and women as a treatment option for the correction of nasolabial folds. Additional information about Artes Medical and ArteFill is available at www.artesmedical.com and www.artefill.com.

Forward-Looking Statements

This news release may contain forward-looking statements that are based on the Company's current beliefs and assumptions and on information currently available to its management. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause the Company's actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. As a result of these risks, uncertainties and other factors, which include the Company's history of net losses, its reliance on its sole FDA-approved product, ArteFill, its limited experience in commercializing ArteFill, and its ability to receive FDA approval to claim that the aesthetic benefits of ArteFill extend beyond six months, readers are cautioned not to place undue reliance on any forward-looking statements included in this press release. A more extensive set of risks and uncertainties is set forth in the Company's SEC filings available at www.sec.gov. These forward-looking statements represent beliefs and assumptions only as of the date of this news release, and the Company assumes no obligation to update these forward-looking statements publicly, even if new information becomes available in the future.

Artes Medical® and ArteFill® are registered trademarks of Artes Medical, Inc.


Source: Artes Medical

Issuer of this News Release is solely responsible for its content.
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