TransEnterix Schedules     Fourth Quarter and Fiscal Year 2015 Financial and Operating Results     Conference Call for March 3, 2016
  RESEARCH TRIANGLE PARK,     N.C.--(BUSINESS WIRE)--February 18, 2016--
  TransEnterix, Inc. (NYSE     MKT:TRXC) announced today that it plans to release fourth quarter and     fiscal year 2015 financial and operating results after the market closes     on Thursday, March 3, 2016. Todd M. Pope, President & Chief Executive     Officer and Joseph P. Slattery, Executive Vice President and Chief     Financial Officer will host a conference call to discuss these results     starting at 4:30 pm Eastern Time the same day. The call will be     concurrently webcast.
  To listen to the conference call on your     telephone, please dial, 888-505-4369 for domestic callers and 719-457-0820     for international callers, and reference TransEnterix Call approximately     ten minutes prior to the start time. To access the live audio webcast or     archived recording, use the following link      ir.transenterix.com. The replay will be available on the     Company's website.
  About TransEnterix
  TransEnterix is a     medical device company that is pioneering the use of robotics to improve     minimally invasive surgery by addressing the clinical and economic     challenges associated with current laparoscopic and robotic options. The     company is focused on the development and commercialization of the     SurgiBot(TM) System, a single-port, robotically enhanced laparoscopic     surgical platform, and the commercialization of ALF-X(R), a multi-port     robotic system that brings the advantages of robotic surgery to patients     while enabling surgeons with innovative technology such as haptic feedback     and eye tracking camera control. The SurgiBot System is not yet available     for sale in any market. The ALF-X has been granted a CE Mark but is not     available for sale in the US. For more information, visit the TransEnterix     website at  www.transenterix.com.
  View source version on     businesswire.com: businesswire.com
  CONTACT:     TransEnterix, Inc.
  Investor Contact:
  Mark Klausner,     443-213-0501
  transenterix@westwicke.com
  or
  Media     Contact:
  Mohan Nathan, 919-917-6559
  mnathan@transenterix.com     =======================================================     - Continue to anticipate     SurgiBot FDA clearance by the end of the first quarter of 2016 -
  -     Strengthens balance sheet with $18M of equity raised -
  RESEARCH     TRIANGLE PARK, N.C.--(BUSINESS WIRE)--February 10, 2016--
  TransEnterix,     Inc. (NYSE MKT: TRXC), a medical device company that is pioneering the use     of robotics and flexible instruments to improve minimally invasive     surgery, today announced the following:
  -- Completes FDA Response.     TransEnterix has successfully completed its response to the U.S. Food and     Drug Administration (FDA) related to the pending 510(k) application     submitted for clearance of the company's SurgiBot(TM) System. --     Strengthens Balance Sheet. Since September 30, 2015, the Company has     raised $18 million(1) in net proceeds at an average price of $3.23 per     share under its $25 million "at-the-market" (ATM) equity sales facility     that was established in February 2015. There is no further availability     under this facility. The proceeds from these sales will be utilized to     continue to support investments for the commercialization of the ALF-X(R)     system in Europe, as well as the SurgiBot in the United States, following     FDA clearance. -- Files New ATM Facility. Following the successful     completion of the prior ATM facility, the Company has entered into a new     ATM facility that allows it the option to raise up to $43.6 million in     equity from time to time through January 2017. The Company has no     obligation to sell any shares under this facility.
  "We are pleased     to have completed our response to the FDA and strengthened our balance     sheet," said TransEnterix President and CEO, Todd M. Pope. "We continue to     expect FDA clearance for the SurgiBot System in the first quarter of this     year, and our cash position allows us to accelerate our transition to     commercializing both the ALF-X and the SurgiBot."
  (1) Includes     trades that have been processed but not yet settled as of the date of this     press release.
  About TransEnterix
  TransEnterix is a medical     device company that is pioneering the use of robotics to improve minimally     invasive surgery by addressing the clinical and economic challenges     associated with current laparoscopic and robotic options. The company is     focused on the development and commercialization of the SurgiBot(TM)     System, a single-port, robotically enhanced laparoscopic surgical     platform, and the commercialization of ALF-X(R), a multi-port robotic     system that brings the advantages of robotic surgery to patients while     enabling surgeons with innovative technology such as haptic feedback and     eye tracking camera control. The SurgiBot System is not yet available for     sale in any market. The ALF-X has been granted a CE Mark but is not     available for sale in the US. For more information, visit the TransEnterix     website at  www.transenterix.com.
  Forward Looking Statements
  This     press release includes statements relating to the SurgiBot System, the     ALF-X(R) System and our current regulatory and commercialization plans for     these products. 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, including whether we     will achieve clearance for the SurgiBot System from the FDA in the first     quarter of this year and whether our cash position allows us to accelerate     our transition to commercializing both the ALF-X and the SurgiBot. For a     discussion of the most significant risks and uncertainties associated with     TransEnterix's business, please review our filings with the Securities and     Exchange Commission (SEC), including our Quarterly Report on Form 10-Q     filed on November 9, 2015 and our other filings we make with the SEC. You     are cautioned not to place undue reliance on these forward looking     statements, which are based on our expectations as of the date of this     press release and speak only as of the origination date of this press     release. We undertake no obligation to publicly update or revise any     forward-looking statement, whether as a result of new information, future     events or otherwise.
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