OnFlex™ Synthetic mesh OnFlex™ Mesh

OnFlex™ Mesh, Large, 10.2 cm x 15.7 cm

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Same proven technique with improved mesh.

Bard© OnFlex™ Mesh was specifically designed to fit the inguinal anatomy during preperitoneal placement. It offers extended medial and inferior coverage for direct and femoral hernia spaces.

Features and Benefits
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GTIN - Case






Large with pocket 4.0" x 6.2" (10.2cm x 15.7cm)


GTIN - Case 00801741074431 1


Quantity 1/cs.

Product Basic Specification

Dimensions Large with pocket 4.0" x 6.2" (10.2cm x 15.7cm)
Electronic Instructions for Use (eIFUs)
Frequently Asked Questions
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North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints

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1. Brown C, Finch J. Which mesh for hernia repair? Annals of The Royal College of Surgeons of England 2010;92(4):272-278.

* Observed in preclinical model, which may not correlate to performance in humans.


The OnFlex™ Mesh is indicated for use in the reinforcement of soft tissue where weakness exists, such as in the repair of inguinal hernias.


Use of this device is contraindicated for infants, children, or pregnant women, whereby future growth will be compromised by use of such mesh material. Literature reports that there is a possibility for adhesion formation when polypropylene is placed in direct contact with the bowel or viscera.


The use of any synthetic mesh or patch in a contaminated or infected wound can lead to fistula formation and/or extrusion of the mesh and is not recommended. If an infection develops, treat the infection aggressively. Consideration should be given regarding the need to remove the mesh. Unresolved infection may require removal of the mesh.

Do not cut or reshape the Onflex™ Mesh, except at the opening in the interrupted SorbaFlex™ PDO monofilament, to accommodate the spermatic cord and outside of the blue limit line in the lateral portion of the mesh, as this could affect its effectiveness. Care should be taken not to cut or nick the SorbaFlex™ PDO monofilament.


Care should be taken not to cut or nick the SorbaFlex™ PDO monofilament.

Adverse Reactions

Possible complications may include, but are not limited to, seroma, adhesion, hematoma, pain, infection, inflammation, extrusion, erosion, migration, fistula formation and recurrence of the hernia or soft tissue defect. If the SorbaFlex™ PDO monofilament is cut or damaged, additional complications may include, but are not limited to, bowel or skin perforation and infection.