TransEnterix soars after FDA clears robot surgical device

The FDA has deemed TransEnterix's device to be substantially equivalent to one sold by Intuitive Surgical.

TransEnterix Surgical has received FDA clearance to sell its robotically assisted surgical device, sparking a 75% jump in its stock price. The green light marks the arrival of a rare new entrant to the field of abdominal surgery robotics.

Research Triangle Park, North Carolina-based TransEnterix has designed its device, the Senhance System, to make it easier for doctors to perform laparoscopic surgery. The surgeon sits at a console equipped with a monitor showing the operating area and moves three robotic arms using a joystick. Haptic feedback is provided so the surgeon can gauge the stiffness of tissue grasped by the robotic arms. Eye-sensing technology controls the camera.

Collectively, the features are designed to enable surgeons to see and accurately grasp, cut, suture and otherwise manipulate tissues from a more comfortable position. TransEnterix thinks this sets the Senhance System up to fill a gap in the market.  


Overcoming Risk in Oncology Drug Development

Oncology drug development is full of potential obstacles and risks, and you must carefully plan each step. Download this whitepaper for tips on finding the fast track. Premier Research. Built for Biotech.

“Millions of surgical procedures in the U.S. are performed each year laparoscopically with basic manual tools that limit surgeons’ capability, comfort and control,” TransEnterix CEO Todd Pope said in a statement. “New choices are needed that enhance the senses, control and comfort of the surgeon, minimize the invasiveness of surgery for the patient and maximize value for the hospital.”

RELATED: TransEnterix opens $44M equity facility as it awaits FDA go-ahead to launch surgical robot

TransEnterix picked up the 510(k) clearance on the strength of results from a 150-patient clinical trial. Investigators used the Senhance System to perform a range of gynecological procedures and compared the outcomes to historical results achieved by older robotically assisted devices. 

The FDA also reviewed results from 45 patients who underwent colorectal procedures, real-world evidence and tests performed under simulated worst-case conditions before ruling that the device is substantially equivalent to Intuitive Surgical’s da Vinci Si in colorectal and gynecological surgeries.

TransEnterix will now take this data to surgeons and healthcare systems in an attempt to get them to adopt its technology over those sold by the incumbent, Intuitive Surgical. The availability of a technology from a new company is a novel experience for these buyers. TransEnterix thinks it is the first new entrant to the abdominal surgical robotics sector since 2000.

Suggested Articles

The FDA approved the first spinal tether to correct the most common form of scoliosis—a ropelike implant that pulls the vertebrae into shape.

Agilent launched a new analyzer for research that observes cell behavior in real time while also collecting biosensor information.

Five years after Congress passed a law to reduce unnecessary MRIs and CT scans, federal officials have yet to implement it.