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Anchora Medical Receives FDA clearance for its Su2ura® Minimally-Invasive Surgical Suturing Device

The Su2ura® Approximation Device automates and simplifies the technically challenging way endoscopic suturing is currently performed during minimally-invasive surgery for improved care.


News provided by

Anchora Medical

Jul 01, 2021, 08:55 ET

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The Su2ura Approximation Device for Minimally Invasive Surgical Suturing
The Su2ura Approximation Device for Minimally Invasive Surgical Suturing

CAESAREA, Israel, July 1, 2021 /PRNewswire-PRWeb/ -- Anchora Medical, an Israel-based medical device company, announced today that it has received 510(k) clearance from the United States (U.S.) Food and Drug Administration (FDA) to market its Su2ura® Approximation Device, an innovative, automated suturing device used in laparoscopic surgery, for the placement of interrupted or running stitches in soft tissue.

Today, standard laparoscopic suturing during Minimal-Invasive Surgery (MIS) is complex and technically challenging. Surgeons face altered depth perception, two-dimensional vision, a small working field, and use long instruments, where the needle driver is far from the surgeon's hand, making precision suturing challenging.

Similar to sewing machines becoming a household item, Anchora Medical was founded to extend these same ideas to bring automated and simplified suturing to minimally invasive surgery. We are delighted the Su2ura® has received FDA clearance to turn this vision into a reality.”

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The Su2ura® Approximation Device enables a simple, automated single-trigger operation that combines simplicity, strength, and durability of sutures during MIS. By simplifying the suturing procedure, the Su2ura® Approximation Device aims to shorten operation time, lower costs, reduce risks and improve clinical outcomes.

The proprietary, patent protected Su2ura® Approximation Device incorporates tiny stainless-steel smart anchors threaded on a surgical thread to create sutures seamlessly adjusted by the surgeon for precision suturing in small spaces. It is a sterile single-use device operated through a 5 mm laparoscopic port.

The Su2ura® device has been used in human trials, performing laparoscopic procedures and successfully closing primary umbilical hernia defects prior to mesh fixation. The surgeries are being performed in two medical centers.

Anchora's CEO, Yoni Epstein, commented: "We are proud to receive FDA clearance for our novel Su2ura® Approximation Device which will set a new standard in the way laparoscopic and endoscopic suturing is performed during MIS. The FDA clearance signifies a critical milestone in our development and will enable us to move forward to commercialization."

Anchora Chairman, Dr. Shimon Eckhouse, added: "Similar to sewing machines becoming a household item, Anchora Medical was founded in 2014 to extend these same ideas to bring automated and simplified suturing to minimally invasive surgery. We are delighted the Su2ura® has received FDA clearance to turn this vision into a reality."

Among Anchora's investors are HOYA Corporation (ADR: HOCPY, TYO: 7741), Dr. Shimon Eckhouse, Alon Medtech Ventures, Tal Capital, and other private investors.

About Anchora Medical:
Anchora Medical is a privately-held medical device company based in Israel. Its platform technology is devoted to changing suturing in both laparoscopic and endoscopic procedures. Anchora was founded as part of the IIA, Alon Medtech incubator. For more information, visit: http://www.anchora-medical.com .

Media Contact

Viki Gronau, Joya Marketing, +972 542587278, [email protected]

Yoni Epstein, Anchora Medical, +972547776615, [email protected]

SOURCE Anchora Medical

Related Links

http://www.anchora-medical.com/

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Yoni Epstein, Co-founder & CEO of Anchora Medical
Yoni Epstein, Co-founder & CEO of Anchora Medical
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Yoni Epstein, Co-founder & CEO of Anchora Medical Anchora Medical logo

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