EDAP Announces FDA Breakthrough Device Designation for Focal One in the Treatment of Deep Infiltrating Rectal Endometriosis
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EDAP TMS SA announced its Focal One platform received FDA Breakthrough Device designation for treating deep infiltrating rectal endometriosis. Previously, in June 2018, the FDA cleared Focal One for prostatic tissue ablation.

March 04, 2024 | 12:02 pm
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EDAP TMS SA's Focal One platform received FDA Breakthrough Device designation for the treatment of deep infiltrating rectal endometriosis.
Receiving FDA Breakthrough Device designation is a significant positive development for EDAP TMS SA. It not only validates the company's technology but also potentially accelerates the adoption and insurance coverage of Focal One for treating deep infiltrating rectal endometriosis. This news is likely to be viewed positively by investors, potentially leading to a short-term increase in EDAP's stock price.
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