Press Release
Asensus Surgical Receives FDA 510(k) Clearance for Senhance Surgical System in Urology
“This FDA clearance marks another milestone for
Healthcare providers perform upwards of 185,000 urological surgical procedures each year in
The Senhance Surgical System is designed to increase surgeon control and reduce variability through Augmented Intelligence and deep learning capabilities.
About
Forward-Looking Statements
This press release includes statements relating to Asensus, the Senhance Surgical System and the FDA’s clearance for an expanded indication to treat adult and pediatric Urology patients with the Senhance Surgical System. These statements and other statements regarding our future plans and goals constitute "forward looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, and are intended to qualify for the safe harbor from liability established by the Private Securities Litigation Reform Act of 1995. Such statements are subject to risks and uncertainties that are often difficult to predict, are beyond our control and which may cause results to differ materially from expectations and include whether the FDA clearance will represent another expansion in our market, and whether the Senhance Surgical System’s precision and advanced digital capabilities make it uniquely suited for urological procedures, offering surgeons the benefit of digital tools and smaller instrumentation. For a discussion of the risks and uncertainties associated with the Company’s business, please review our filings with the
ASENSUS SURGICAL CONTACT:
INVESTORS
ICR Westwicke
invest@asensus.com
443-213-0499
MEDIA
AsensusPR@matternow.com
617-874-5488
*Urology Market data forecasted for 2023 from DRG Clarivate Laparoscopic Market Insights -
A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/de156f18-f140-4fc1-86fd-ee125390d46e
Source: Asensus Surgical, Inc.