Evidence-supported clinical uses and emerging applications for superior wound healing outcomes
Kerecis products have demonstrated clinical efficacy across multiple wound types with peer-reviewed evidence supporting their use in standard clinical practice.
Clinical Overview: Kerecis Shield is specifically designed and FDA-cleared for diabetic foot ulcer management, addressing the unique metabolic and vascular challenges of diabetic wounds.
Product Recommendation: Kerecis Shield (Silicone or Standard variants) - the silicone contact layer reduces pain and provides optimal moisture management for sensitive diabetic foot tissue.
Key Evidence:
Clinical Overview: Kerecis MariGen line supports rapid granulation tissue formation and epithelialization in chronic venous ulcers, which frequently fail conventional dressing approaches.
Product Recommendation: Kerecis MariGen (Fenestrated or Solid variants) for optimal exudate management and vascularization support in venous wounds.
Key Evidence:
Clinical Overview: Kerecis GraftGuide is optimized for thermal injuries, providing superior scar outcomes and faster re-epithelialization compared to traditional burn dressings.
Product Recommendation: Kerecis GraftGuide (Solid or Micro variants) for second-degree and full-thickness burns; Mano (hand-shaped) for specialized hand burn coverage.
Key Evidence:
Clinical Overview: Kerecis SurgiClose addresses post-operative defects including Mohs surgical wounds, split-thickness donor sites, and surgical excision sites requiring rapid re-epithelialization.
Product Recommendation: Kerecis SurgiClose (Standard or Silicone variants) for post-Mohs reconstruction; Meshed 2:1 for larger donor sites requiring expanded coverage.
Key Evidence: Well-established clinical practice demonstrates that fish skin grafts significantly accelerate wound closure compared to traditional post-surgical management, with improved aesthetic outcomes particularly valued in dermatologic and cosmetic procedures.
Clinical Overview: Kerecis MariGen is indicated for pressure ulcer management across stages II through IV, addressing the deep tissue damage and biofilm challenges characteristic of pressure injuries.
Product Recommendation: Kerecis MariGen (Solid for deep wounds; Expanse for large surface areas) combined with pressure relief and specialized wound care protocols.
Key Evidence: Clinical practice demonstrates that fish skin grafts support granulation tissue formation and epithelialization in pressure ulcers, particularly in patients with limited healing capacity due to age or comorbidities.
Clinical Overview: Kerecis SurgiBind Tendon Protect provides specialized reinforcement for exposed or repaired tendons, supporting surgical outcomes in complex extremity reconstruction.
Product Recommendation: Kerecis SurgiBind Tendon Protect for tendon repair sites, soft tissue barriers, and complex surgical reconstructions requiring structural support.
These applications are supported by peer-reviewed scientific literature but may not represent FDA-cleared indications. Healthcare providers should exercise clinical judgment when considering these applications.
Clinical Application: Treatment of pediatric traumatic wounds, surgical defects, and partial-thickness injuries with minimal scarring.
Mechanism: Fish skin's natural composition and bioactive properties are ideal for pediatric patients, supporting rapid epithelialization while minimizing the hypertrophic scarring that frequently affects developing skin.
Key Evidence:
Product Recommendation: Kerecis MariGen Solid for pediatric traumatic wounds; SurgiClose for post-surgical pediatric defects.
Clinical Application: Management of difficult-to-heal wounds in patients with peripheral arterial disease, diabetic neuropathy with vascular compromise, and chronic critical limb ischemia.
Mechanism: Fish skin's high omega-3 content and neovascularization-promoting properties may enhance healing even in severely compromised vascular environments through activation of pro-resolving inflammatory pathways.
Key Evidence:
Product Recommendation: Kerecis MariGen (Fenestrated variant for optimal exudate management) combined with vascular intervention and aggressive cardiovascular risk factor management.
Clinical Application: Integration of Kerecis with negative pressure wound therapy (NPWT) for complex, heavily exudative wounds requiring mechanical and biological support.
Mechanism: The combination of fish skin's bioactive scaffold with negative pressure provides simultaneous mechanical wound conditioning and biological healing stimulation, potentially synergizing outcomes.
Key Evidence:
Product Recommendation: Kerecis MariGen Fenestrated as the base scaffold under NPWT systems, allowing optimal fluid management and tissue contact.
Clinical Application: Coverage of exposed critical structures (tendons, nerves, bone) in hand and upper extremity trauma with rapid incorporation and minimal scarring.
Mechanism: Fish skin's acellular matrix rapidly incorporates into surrounding tissues while providing protective coverage, enabling early mobilization and functional recovery in complex hand injuries.
Key Evidence:
Product Recommendation: Kerecis GraftGuide Mano (hand-shaped variant) or SurgiBind Tendon Protect for specialized coverage of exposed critical structures.
Clinical Application: Management of blast injuries, crush injuries, and complex contaminated wounds in military, disaster, and austere medical settings with limited standard care resources.
Mechanism: Fish skin's antimicrobial properties, reduced infection risk, and minimal processing requirements make it well-suited for challenging wound environments with high infection risk.
Key Evidence:
Product Recommendation: Kerecis MariGen (shelf-stable, minimal refrigeration requirements) for field hospital and austere care applications.
Clinical Application: Wound bed preparation and reconstruction following necrotizing fasciitis debridement, facilitating transition from acute infection management to healing phase.
Mechanism: Fish skin's antimicrobial and anti-inflammatory properties support rapid wound bed preparation in post-necrotizing fasciitis wounds, reducing infection recurrence risk while promoting granulation tissue formation.
Product Recommendation: Kerecis MariGen Solid for deep tissue defects; SurgiClose for large debridement sites requiring extensive coverage.
Clinical Application: Specialized coverage for complex hand wounds including exposed tendons, joints, and critical anatomic structures.
Mechanism: The hand-shaped GraftGuide Mano product provides anatomically optimized coverage that maintains hand form and function while enabling rapid integration and minimizing scar contracture.
Product Recommendation: Kerecis GraftGuide Mano (hand-shaped specialized variant) for complex hand wound coverage with superior anatomic precision.
Kerecis fish skin grafts leverage multiple biological mechanisms that address the fundamental challenges of wound healing across diverse clinical applications.
The three-dimensional collagen and elastin architecture provides a permissive scaffold for host cell infiltration, fibrovascular network formation, and tissue remodeling — addressing the fundamental need for structural support in all wound types. The intact 3D structure is preserved through the gentle EnviroIntact™ process, making it homologous to human skin.
EPA and DHA in fish skin activate specialized pro-resolving mediator (SPM) pathways that downregulate pro-inflammatory cytokine production and promote the transition from inflammatory to proliferative healing phases — critical for chronic wound resolution. Fish skin facilitates 20x more cell ingrowth than amniotic tissue.
The bioactive scaffold and immunomodulatory properties stimulate robust neovascularization, improving oxygen and nutrient delivery to healing tissues — particularly important in ischemic and chronic wound environments. The natural porosity enables rapid ingrowth of fibroblasts and blood vessels.
Fish skin's inherent antimicrobial characteristics reduce bacterial colonization and infection risk — a 0.88% infection rate was documented across 114 patients in a systematic review. This addresses a primary impediment to healing in contaminated and biofilm-prone wounds.
Successful Kerecis integration requires thoughtful product selection based on wound type, anatomic location, and specific clinical goals.
Some applications listed in this document are based on emerging research and peer-reviewed literature but may not represent FDA-cleared indications for all Kerecis products. The establishment, FDA clearance status, and evidence level vary by product variant and application.
Healthcare providers should exercise independent clinical judgment when considering any application. This information does not constitute medical advice, and individual clinical decisions should be made in consultation with appropriate medical professionals, current clinical evidence, and institutional protocols.
For current FDA clearance status and approved indications, please consult the product's 510(k) summaries and labeling documentation, available through the FDA device database.
Discover how Kerecis products can optimize outcomes for your patients across diverse wound care applications.