Press Release
TransEnterix Provides 2017 Year End Corporate Update
"2017 was a transformational year for
Senhance System Revenue
During the quarter ending
The company currently has received one European Senhance System order
that it expects to deliver and recognize revenue for in the quarter
ending
Product Portfolio
During 2017, the company completed the following product portfolio initiatives:
- Obtained Senhance System FDA 510(k) clearance for use in colorectal and gynecologic laparoscopic surgery
- Obtained CE mark and began commercializing the world's first robotic micro-laparoscopic (3 millimeter) instruments
-
Expanded list of compatible visualization and fluorescence systems to
include systems from Stryker, Novadaq (Stryker), Conmed and
Richard Wolf - Filed approximately 40 new US patent applications. The Company's patent portfolio now includes approximately 93 issued patents, 25 of which are US Patents, as well as approximately 92 pending applications, 54 of which are US applications.
The Company expects to complete the following product portfolio initiatives in 2018:
- Expand the Senhance System US FDA clinical indications to include hernia and gallbladder, doubling the total addressable market
- Launch new ultrasonic energy device
- Launch new five-millimeter articulating instrument platform
SurgiBot Global System Agreement
On
The agreement provides the Company with proceeds of at least
This agreement transfers ownership of the SurgiBot System assets, while
the Company retains the option to distribute or co-distribute the
SurgiBot system outside of
Balance Sheet
As of
As of
About
Forward-Looking Statements
This press release contains "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, which 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, including whether we will be able to build upon our
momentum and drive the global adoption of the Senhance in 2018; whether
we will deliver and recognize revenue from the sale of a European
Senhance System in the 2018 first quarter; whether we will expand the
Senhance System US FDA clinical indications to include hernia and
gallbladder; whether we will launch a new ultrasonic energy device,
whether we will launch a new five-millimeter instrument platform;
whether
View source version on businesswire.com: http://www.businesswire.com/news/home/20180108005939/en/
For
Investors:
invest@transenterix.com
or
Media:
joanna@greymattermarketing.com
Source:
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