Modified OnFlex Mesh, 3.4" x 5.6" (8.6 cm x 14.2 cm), Medium

Modified OnFlex Mesh, 4.0" x 6.2" (10.2 cm x 15.7 cm), Large

3DMax MID Anatomical Mesh, 12 cm x 17 cm (5" x 7"), Extra Large, Left

3DMax MID Anatomical Mesh, 12 cm x 17 cm (5" x 7"), Extra Large, Right

Phasix ST Mesh, 10 cm x 10 cm (4" x 4"), Square

Phasix ST Mesh, 10 cm x 15 cm (4" x 6"), Rectangle

Phasix ST Mesh, 10 cm x 20 cm (4" x 8"), Rectangle

Phasix ST Mesh, 20 cm x 25 cm (8" x 10"), Rectangle

Phasix ST Mesh, 25 cm x 30 cm (10" x 12"), Rectangle

Phasix ST Mesh, 30 cm x 35 cm (12" x 14"), Rectangle

Phasix ST Mesh with Echo 2 Positioning System, 11 cm (4.5"), Circle

Phasix ST Mesh with Echo 2 Positioning System, 15 cm (6"), Circle

Phasix ST Mesh with Echo 2 Positioning System, 20 cm (8"), Circle

Phasix ST Mesh with Echo 2 Positioning System, 10 cm x 15 cm (4" x 6"), Ellipse

Phasix ST Mesh with Echo 2 Positioning System, 15 cm x 20 cm (6" x 8"), Ellipse

Phasix ST Mesh with Echo 2 Positioning System, 15 cm x 25 cm (6" x 10"), Oval

Phasix ST Mesh with Echo 2 Positioning System, 18 cm x 23 cm (7" x 9"), Ellipse

Phasix ST Mesh with Echo 2 Positioning System, 20 cm x 25 cm (8" x 10"), Ellipse

Phasix ST Mesh with Echo 2 Positioning System, 25 cm x 33 cm (10" x 13"), Ellipse

Phasix ST Mesh with Echo 2 Positioning System, 30 cm x 35 cm (12" x 14"), Ellipse

Phasix ST Mesh with Open Positioning System, 11 cm (4.5"), Circle

Phasix ST Mesh with Open Positioning System, 8 cm x 12 cm (3" x 5"), Oval

Phasix ST Mesh with Open Positioning System, 10 cm x 15 cm (4" x 6"), Oval

Phasix ST Mesh with Open Positioning System, 15 cm x 20 cm (6" x 8"), Oval

Phasix ST Mesh with Open Positioning System, 15 cm x 30 cm (6" x 12"), Oval

Phasix ST Mesh with Open Positioning System, 20 cm x 25 cm (8" x 10"), Oval

Phasix ST Mesh with Open Positioning System, 25 cm x 30 cm (10" x 12"), Oval

Phasix ST Mesh with Open Positioning System, 30 cm x 35 cm (12" x 14"), Oval

Ventralight ST Mesh with Echo 2 Positioning System, 4.5" (11 cm), Circle

Ventralight ST Mesh with Echo 2 Positioning System, 6" (15 cm), Circle

Ventralight ST Mesh with Echo 2 Positioning System, 8" (20 cm), Circle

Ventralight ST Mesh with Echo 2 Positioning System, 4" x 6" (10 x 15 cm), Ellipse

Ventralight ST Mesh with Echo 2 Positioning System, 6" x 8" (15 x 20 cm), Ellipse

Ventralight ST Mesh with Echo 2 Positioning System, 6" x 10" (15 x 25 cm), Oval

Ventralight ST Mesh with Echo 2 Positioning System, 7" x 9" (18 x 23 cm), Ellipse

Ventralight ST Mesh with Echo 2 Positioning System, 8" x 10" (20 x 25 cm), Ellipse

Ventralight ST Mesh with Echo 2 Positioning System, 10" x 13" (25 x 33 cm), Ellipse

Ventralight ST Mesh with Echo 2 Positioning System, 12" x 14" (30 x 35 cm), Ellipse

The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.

The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device is used to deploy the implant into the prepared hernia defect site.

Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.

Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.

Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.

Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.

Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used for management and protection of tendon injuries in which there has been no substantial loss of tendon tissue. Minimizes tissue attachment to the device in case of direct contact with the tissues. Also indicated for reinforcement of soft tissues repaired by suture or suture anchors, during tendon repair surgery. Reinforces soft tissue and provides a remodelable scaffold that is replaced by the patient’s own soft tissue. The device is indicated for open and laparoscopic/endoscopic procedures.

Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used for management and protection of tendon injuries in which there has been no substantial loss of tendon tissue. Minimizes tissue attachment to the device in case of direct contact with the tissues. Also indicated for reinforcement of soft tissues repaired by suture or suture anchors, during tendon repair surgery. Reinforces soft tissue and provides a remodelable scaffold that is replaced by the patient’s own soft tissue. The device is indicated for open and laparoscopic/endoscopic procedures.

For temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries are necessary.

For temporary bridging of fascial defects where primary closure is not possible, including but not limited to, abdominal compartment syndrome.