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Description

Smart design.†,1–6 Smart handling.†,‡,§,◊,¶,1,5,7–8 Smart repair.†,‡,#,∞,††,1,2,7,9–11

The Symbotex™ composite mesh can be used for minimally invasive surgery, such as conventional laparoscopic surgery and robotically-assisted hernia surgery, and open ventral hernia repair.12,13 Symbotex™ mesh brings improved ease of use as well as optimal repair performance for your patients, with excellent tissue integration and minimized visceral attachments.

Symbotex™ composite mesh is available in a large variety of shapes and sizes for laparoscopic hernia repair, with specific subranges dedicated to laparoscopic and open surgery.


Refer to the indications for use for complete instructions.

† Based on preclinical animal studies and benchtop studies. Animal data and benchtop testing are not necessarily indicative of human clinical outcomes.

‡ Based on preclinical animal studies. Animal data is not necessarily indicative of human clinical outcomes.

§ If the mesh is not cut (refer to instructions for use). Particular attention should be paid not to cut the green marking. It may no longer be centered and lose its functions if the mesh is trimmed.

◊ Not applicable for SYM-OS codes. Except in cases where transfacial sutures are used as well as meshes in open approach.

¶ Based on surgeon feedback and that 4/6 answers good or very good clinging effect.

# Tissue reinforcement and integration are indirectly assessed in clinical studies by the reported low recurrence rates.

∆ Minimization of visceral adhesions are indirectly assessed in clinical studies by the absence of adhesion complications. 

∞ Based on benchtop studies. Benchtop testing data is not necessarily indicative of human clinical outcomes. 

†† Clinical outcomes expressed by low hernia recurrence rates and improvement in the quality of life.


  1. Based on internal test report 0901CR247b, Design verification report. July 2013.
  2. Based on internal test report 163005, Evaluate local tissue effects and tissue integration of Symbotex™ composite mesh versus Parietex™ optimized composite mesh after laparoscopic ventral repair. October 2013.
  3. Based on internal test report 162750, Evaluating local tissue effects, tissue integration and minimizing tissue attachment performance of Symbotex™ composite mesh versus Parietex™ optimized composite mesh. May 2013.
  4. Based on internal test report E41335/E41336CR022a, Design verification report. May 2014.
  5. Based on internal test report 0901CR252a, Preclinical study on pigs by surgeons for design validation of Symbotex™. June 2013.
  6. Based on internal report, Size and shape comparison chart. September 2013.
  7. Gillion JF, Lepere M, Barrat C, et al. Two-year patient-related outcome measures (PROM) of primary ventral and incisional hernia repair using a novel three-dimensional composite polyester monofilament mesh: the SymCHro registry study. Hernia. 2019;23(4):767−781. 
  8. Based on internal test report 0901CR261a, Observed clinging effect of Symbotex™ during design validation. July 2013.
  9. Abouzeid T, Mohammed A. Laparoscopic intraperitoneal onlay mesh for Spigelian hernia repair a prospective study. Egyptian J Surg. 2018;37(4):445−452.
  10. Design verification report 0901CR247b. July 2013. The report demonstrates the minimizing tissue adhesion performance of the mesh at four weeks.
  11. Based on internal test report E41335/E41336CR022a, Design verification report. March 2018.
  12. Based on internal test report TEX-FP-068c, Symbotex™ composite mesh, Ø08mm trocar compatibility. July 2019.
  13. Based on internal report TVX-20-020-CR-0001a, Robotically-assisted laparoscopic ventral hernia surgery with Symbotex™ composite mesh — impact on usability engineering. February 2021.

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Find more information, including other available configurations, for Symbotex™ composite mesh.

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