Overview

Consistent port-site closures without removing the port1,‡,§

The VersaOne™ fascial closure system is a unique all-in-one1,† solution that serves as a trocar and a fascial closure device to deliver:

  • Consistent port-site closure1,‡
  • Added procedural efficiency1,§
  • Ease of use1,§

EVEN A SINGLE PORT SITE HERNIATION IS A BIG CHALLENGE

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FEATURES

Access and closure with a single device1,†

The VersaOne™ fascial closure system brings consistent suture placement to laparoscopic closures.1,§ It also:

  • Eliminates the need to remove the trocar before closing1,‡
  • Makes reinsufflation unnecessary — pneumoperitoneum can be maintained throughout the procedure2,‡
  • Allows tissue layers to remain aligned2,‡

Key features

The cannula window and guide help facilitate closure of the fascia at 5 mm on either side of the cannula defect3,Ω

  • The black visual indicators  aid  in  consistent suture placement1,2,§,††
  • The needle tip and grasping features of the suture passer allow for subcutaneous insertion and grasping of the suture
  • The low-profile ergonomic obturator is available in an optical or bladed tip
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Order Information
Order Code Description Unit of Measure Quantity
ONB12STFCS VersaOne™ Fascial Closure System Optical Trocar Box 6
B12STFCS VersaOne™ Fascial Closure System Bladed Trocar Box
6
FCSPASS VersaOne™ Fascial Closure System Reusable Suture Passer Box 1

Order Information

Award-Winning Design

The Medical Design Excellence Awards named our VersaOne™ fascial closure system a Gold Winner in their ER and OR Tools category. 

Medical Design Excellence Awards
  • †Based on cadaver usability lab with 16 surgeons (13 of 16 surgeons agreed). The two devices are: a standard trocar and a fascial closure system. Preclinical results may not correlate with clinical performance in humans.

  • ‡Based on usability lab with 16 surgeons (16 of 16 surgeons agreed). Preclinical results may not correlate with clinical performance in humans.

  • §Based on usability lab with 16 surgeons (13 of 16 surgeons agreed). Preclinical results may not correlate with clinical performance in humans.

  • ΩBite size determined by bench top testing which evaluated perpendicular distance between the edge of the cannula at the black O-ring point to the center of the suture passer.

  • †† Based on usability lab with 16 surgeons. (14 of 16 surgeons agreed). Preclinical results may not correlate with clinical performance in humans.

  • 1. Based on internal validation report #RE00098009 Rev A, Double Time VersaOne™ fascial closure system Miami lab VOC (3/28). March 28, 2017. 

  • 2. Based on internal validation report #RE00062341 Rev A, Summative usability of project DoubleTime VersaOne™ fascial closure system. Grainger Center for Simulation and Innovation (GCSI), NorthShore University Hospital, Evanston, IL, August 24-25, 2016.

  • 3. Based on internal report #RE00079705, Revision 1, Fascial closure system bite size verification. January 31, 2017.