Wound

Tackle Hard-to-Heal VLUs with MariGen

Promote Faster Wound Closure for Your Patients

Chronic, hard-to-heal venous leg ulcers (VLUs) are devastating for patients who risk losing their mobility, missing work, or withdrawing from social activities.

Backed by industry-leading clinical data, MariGen is designed to help you manage your patients’ toughest VLUs and promote faster wound closure. With its compression-compatible design, available large surface area coverage, and natural components that help expedite the healing process, MariGen has you covered for hard-to-heal VLUs.

MariGen for VLUs

Clinically effective and favorably priced

Compression compatible and available in a wide range of sizes

Backed by comprehensive reimbursement support

Clinically Effective, Favorably Priced

Because there is no known risk of disease transfer from North-Atlantic cod to humans, Kerecis fish-skin grafts are minimally processed with no harsh chemicals or detergents. This gentle processing preserves the fish skin’s natural structure,[1] porosity,[2,3] and natural components,[2,4] which help promote faster and more effective wound healing.

Our products’ clinical efficacy is backed by 100+ peer-reviewed publications, including an ongoing VLU RCT, that demonstrate our ability to fast-track wound healing and close complex ulcers. Check out some of our powerful evidence below:

Natural Components Help Expedite the Healing Process

  • Kerecis’ minimal processing preserves the fish skin’s extracellular matrix (ECM) components, [2] which are often removed during the harsher processing of mammalian tissue replacement products. [5]
  • For example, Kerecis grafts have more natural components than bovine collagen tissue replacement products. [2]
  • Together, these ECM components play key roles in rapidly facilitating angiogenesis, cell migration, and maintaining a bacterial barrier. [6,7]
MariGen

Clinically Proven to Close Complex Ulcers

  • Patients with hard-to-heal lower extremity chronic ulcers saw a 40% decrease in wound surface area and a 48% decrease in wound depth after five weekly applications of Kerecis and secondary dressing. [8]
  • An interim analysis of the THOR trial demonstrates a strong positive trend in using Kerecis to treat nonhealing VLUs: a 25.9% absolute gain in wound closure rates over standard of care alone (47.6% vs 21.7%).* [9]

     *Interim analysis, not statistically significant.

 

Kerecis decreases wound surface area by 40% in 5 weeks [8]

Complementing Kerecis’ strong clinical evidence and patient outcomes, our product prices remain favorable compared to current CMS reimbursement levels. The average cost of our MariGen products fall well below the flat rate of $127.14 per cm2 for hospital outpatient departments, ambulatory surgical centers, physician offices, and home health providers.

Compression Compatible and Available in a Wide Range of Sizes

MariGen is compatible with compression therapy and available in a wide range of sizes and variations to meet your wound-care needs and deliver financial advantages. Our Meshed 2:1 graft can be expanded to cover larger VLUs with less fish-skin material, reducing waste and maximizing cost efficiencies.
Variation Name Product Size Coverage (cm²/Unit)
Standard 3x3.5cm 10.5 cm²
Standard 3 x 7 cm 21 cm²
Standard 5 x 7 cm 35 cm²
Standard 7 x 7 cm 49 cm²
Standard 7 x 10 cm 70 cm²
Fenestrated 3 x 3.5 cm 11 cm²
Fenestrated 3 x 7 cm 21 cm²
Fenestrated 7 x 10 cm 70 cm²
Micro 8 cm² 8
Micro 19 cm² 19
Micro 38 cm² 38
Meshed 2:1 7 x 8 cm up to 101 cm²

Illustrative sizes shown, please contact us for complete product availability.

Backed by Comprehensive Reimbursement Support

Proper documentation is key to ensuring reimbursement for skin substitutes. Kerecis’ field reimbursement team and benefits investigators are available to provide real-time guidance if you need support: reach out anytime to reimbursement@kerecis.com.

Our AI-powered digital platform, Kerecis Current, also provides user-friendly coding and reimbursement guidance to help you align with CMS requirements and streamline your claims and documentation for VLUs. If you have questions, email: current@kerecis.com.

With these streamlined processes and comprehensive reimbursement support, you can focus on what matters most: your patients’ care.

VLU Case Study

Dr. Mark Melendez, MD, MBA
, Plastic and Reconstructive Surgeon

Venous Leg Ulcer

Case Description

Venous leg ulcer on patient’s lower extremity.
Wound was 6-months-old at first application.
Applications: 10

venous-leg-ulcers-1
Initial Wound
venous-leg-ulcers
First application of MariGen
venous-leg-ulcers
1 Month - application #4
venous-leg-ulcers
2 Months - application #7
venous-leg-ulcers
Wound healed at 4 months after 10 applications
Our work has shown that Kerecis intact fish skin is effective in venous leg ulcers that were poorly prepared and have been stalled for long periods of time. We have also found great utility for Kerecis in venous leg ulcers that are undergoing venous surgery. Patients usually note relatively immediate reduction in pain. 
John C Lantis
Dr. John Lantis
, Vascular Surgeon
Mount Sinai Hospital, New York

Download Evidence Summary

A Prospective, Postmarket, Compassionate Clinical Evaluation of a Novel Fish-skin Graft Which contains Omega-3 Fatty Acids for the Closure of Hard-to-heal Lower Extremity Chronic Ulcers

Need more information?

Contact our team to learn how MariGen can help your patients with hard-to heal venous leg ulcers.

Important Information

This website and its content is not intended to provide diagnosis, treatment, or medical advice. Products, services, information, and other content provided on this website, including information provided directly or through links to third-party websites, are for informational purposes only. Information on this website should not be considered a substitute for professional advice from a healthcare provider. Always consult with a physician or other healthcare professional regarding any medical or health-related diagnosis or treatment options.

Products and their variations may not be available in all countries and could be known under different trade names. Products, product names, indications, and claims vary by jurisdiction. Always verify with your local healthcare professional and consult the printed package information before use. Information on this website may not be current and might not reflect the latest product labeling – please refer to latest IFU’s on the website. For questions about product availability, please contact your Kerecis representative or use the contact form on our website.

Products are derived from fish sources and should not be used in patients with a known allergy to fish or sensitivity to fish products. Note that fish allergy is distinct from shellfish allergy. Do not apply fish skin products over infected or deteriorating wounds until the underlying cause has been resolved.

SurgiClose Silicone and Shield products contain silicone and are not suitable for patients with silicone sensitivity.
SurgiBind is not indicated for procedures requiring load-bearing support, such as hernia repair, for intraperitoneal organ contact, or where a bridging effect is needed.
SurgiBind Tendon Protect is not indicated to replace or repair the damaged tendon or to reinforce the strength of any tendon repair.
Always follow the product’s labeling for indications and contraindications.

A surgeon must always rely on their professional clinical judgment when deciding whether to use a specific product for a patient. Kerecis does not dispense medical advice and strongly recommends that surgeons be adequately trained in the use of its products before employing them in surgical procedures. The information provided on this website is intended to demonstrate the product offerings and should not replace the package insert, product label, or instructions for use. For regulatory and medical practice reasons, product availability may vary by market. Contact your Kerecis representative for further clarification.

  • For single patient use only; do not reuse, reprocess, or re-sterilize.
  • Discard any unused portions of the product.
  • Sterile only if the package is unopened and undamaged.
  • Do not use the product if the package seal has been broken, unintentionally opened, or if handling has caused damage or contamination.
  • Do not use after the expiration date printed on the product label or packaging.
  • Remove all non-viable and necrotic tissue prior to application of the product.
  • Remove exudate and control bleeding prior to product application.
  • Do not use in patients with known fish allergies.
  • The product is not designed, sold, or intended for use except as indicated.
  • No clinical trials have been conducted in pediatric, pregnant, or breastfeeding populations.

1

Magnusson S, Baldursson BT, Kjartansson H, Rolfsson O, Sigurjonsson GF. Regenerative and Antibacterial Properties of Acellular Fish Skin Grafts and Human Amnion/Chorion Membrane: Implica- tions for Tissue Preservation in Combat Casualty Care. Mil Med. 2017;182(S1):383-388. doi:10.7205/ MILMED-D-16-00142

2

Yoon J, Dogeon Yoon, Lee H, et al. Wound healing ability of acellular fish skin
and bovine collagen grafts for split-thickness donor sites in burn patients:
Characterization of acellular grafts and clinical application. Int J Biol Macromol.
2022;205:452-461. doi:10.1016/j.ijbiomac.2022.02.055

3

Wang Y, Xu R, He W, et al. Three-Dimensional Histological Structures of the Human Dermis. Tissue Eng Part C Methods. 2015;21(9):932-944.
doi:10.1089/ten.tec.2014.0578

4

Kotronoulas A, Jónasdóttir HS, Sigurðardóttir RS, Halldórsson S, Haraldsson
GG, Rolfsson Ó. Wound healing grafts: Omega-3 fatty acid lipid content
differentiates the lipid profiles of acellular Atlantic cod skin from traditional dermal
substitutes. J Tissue Eng Regen Med. 2020;14(3):441-451. doi:10.1002/
term.3005

5

Crapo PM, Gilbert TW, Badylak SF. An overview of tissue and whole organ
decellularization processes. Biomaterials. 2011;32(12):3233-3243. doi:10.1016/j.
biomaterials.2011.01.057

6

Jiménez-Gastélum GR, Aguilar-Medina EM, Soto-Sainz E, Ramos-Payán R,
Silva-Benítez EL. Antimicrobial Properties of Extracellular Matrix Scaffolds for Tissue Engineering. BioMed Res Int. 2019;2019:1-7. doi:10.1155/2019/964145613

7

Yue B. Biology of the Extracellular Matrix: An Overview. J Glaucoma. 2014;23:S20-S23. doi:10.1097/IJG.0000000000000108

8

Yang CK, et al. A prospective, post-market, compassionate clinical evaluation of
a novel acellular fish-skin graft which contains omega-3 fatty acids for the closure
of hard-to-heal lower extremity chronic ulcers. Wounds, 2016.

9

Serena, et al. Evaluation of intact fish skin grafts plus standard care in thetreatment of venous leg ulcers: an interim analysis of the THOR
trial.  International Journal of Tissue Repair, 2025.