Expanding Hemostatic Foam

LifeFoam
LifeFoam

TACKLE SEVERE NON-COMPRESSIBLE LARGE CAVITY BLEEDING

LifeFoam is a ready-to-use, expanding hemostatic foam in a syringe or spray form, composed of modified chitosan designed to stop bleeding during trauma, orthopedic and plastic surgery bleeding scenarios. Consistent with all LifeTM Surgical Portfolio formulations, the foam also includes the benefit of inherent antimicrobial properties of chitosan.

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LifeFoam is undergoing feasibility studies, and has yet to be evaluated by the FDA.

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Purchase LifeFoam

How Does
LifeFoam
Work?

By providing a matrix for platelet adhesion and aggregation, on contact with fluids, modified chitosan expanding foam allows for mucoadhesion of chitosan to wet tissue, creating a barrier ​that stops bleeding and features the inherent antimicrobial properties of chitosan.

Key
LifeFoam
Features
& Benefits*

LifeFoam
is designed for

  • Ready-to-use
  • Designed to stop severe traumatic bleeding
  • Ideal for traumatic injuries that are non-compressible
  • Ability to fill large cavities in orthopedic and plastic surgery procedures
  • Offers inherent antimicrobial properties of chitosan

See
LifeFoam
in action

For a video demonstration of LifeFoam's hemostatic efficacy, click the images.

PUBLICATIONS

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What Surgeons are
Saying About
LifeFoam

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Position, Company name

Surgical Solutions

Surgical blood loss can lead to complications in the operating room, including increased mortality, morbidity, blood transfusions, infections, longer procedure time and cost. Our LIFE™ Surgical Portfolio of hemostasis options is engineered to solve these problems. We strive to provide safe, efficacious, and cost-effective hemostasis tools for minor, minimal, and moderate surgical bleeding.

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Disclaimer

LifeGel and other LIFE Surgical Portfolio formats, including application devices and tips are currently in development or feasibility. All intended uses and/or indications for use for these medical devices have not been cleared or approved by the FDA.

LifeFoam, including application devices and tips are currently in feasibility. All intended uses and/or indications for use for this medical device have not been cleared or approved by the FDA.

References

* Data on file at Medcura. Based on initial and ongoing development and testing.

** Data on file at Medcura. Ongoing research for time and cost efficiencies.

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