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GORE® ENFORM Biomaterial is not authorized for use in Canada.

GORE® ENFORM Preperitoneal Biomaterial 
Catalogue Number Dimension (cm x cm) 
GBWR0616 6 x 16 
GBWR0816 8 x 16 
GBWR1010 10 x 10 
GBWR1016 10 x 16 
GBWR1620 16 x 20 
GBWR2020 20 x 20 
GBWR2025 20 x 25 
GBWR2030 20 x 30 
GBWR2040 20 x 40 
GBWR2540 25 x 40 
GBWR3030 30 x 30 
GBWR3040 30 x 40 

GORE® ENFORM Intraperitoneal Biomaterial
Catalogue Number Dimension (cm x cm) 
GBFR0816 8 x 16 
GBFR1016 10 x 16 
GBFR1620 16 x 20 
GBFR2025 20 x 25 
GBFR2540 25 x 40 

Sizing, availability, and pricing varies by country.

Please check with your Gore representative for availability. 

IFU Consult instructions

Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly

INDICATIONS FOR USE: The GORE® ENFORM Intraperitoneal Biomaterial is indicated for the reinforcement of soft tissue. This includes use in patients requiring soft tissue reinforcement in plastic and reconstructive surgery. Examples of applications where the GORE® ENFORM Intraperitoneal Biomaterial may be used include hernia repair as suture-line reinforcement, muscle flap reinforcement and general tissue reconstructions.

CONTRAINDICATIONS: The GORE® ENFORM Intraperitoneal Biomaterial is contraindicated for use in reconstruction of cardiovascular defects. The GORE® ENFORM Intraperitoneal Biomaterial is absorbable and contraindicated for use in patients requiring permanent support from the device.

INDICATIONS FOR USE: The GORE® ENFORM Preperitoneal Biomaterial is indicated for use in the reinforcement of soft tissue. This includes use in patients requiring soft tissue reinforcement in plastic and reconstructive surgery. Examples of applications where the GORE® ENFORM Preperitoneal Biomaterial may be used include hernia repair as suture-line reinforcement, muscle flap reinforcement and general tissue reconstructions.

CONTRAINDICATIONS: The GORE® ENFORM Preperitoneal Biomaterial is contraindicated for use in reconstruction of cardiovascular defects. The GORE® ENFORM Preperitoneal Biomaterial is absorbable and contraindicated for use in patients requiring permanent support from the device.