Serinex Medical
Serinex Medical offers DuraDerma, a topical silk-fibroin gel that strengthens skin resilience at high-risk pressure points in bedridden patients to help prevent pressure injuries. Cleared as a Class I 510(k) liquid bandage and skin protectant, it is applied twice daily alongside standard of care. The company is developing Gen 2.0, a next-generation formulation positioned to be the first product cleared to reduce pressure injury formation and progression.
- Medical Devices
- Healthcare Technology
- New Materials
- Biotechnology
- Hardware
Funding
Founders
Founder details are not available yet.
Product
Problem
Pressure injuries are progressive wounds that form in immobilized patients and are a key source of infection. In the U.S., more than 2.5 million cases occur each year, costing over $26.8 billion in care, yet no current products are labeled to reduce the risk of forming a pressure injury or to reduce the risk of progression of early-stage injuries.
Solution
Serinex Medical offers DuraDerma, a topical gel of medical-grade silk fibroin applied alongside standard of care to at-risk points of body contact in bedridden patients. The product acts on intact skin to reinforce its resilience against the mechanical stress and shearing forces that drive pressure injury development and progression, unlike dressings and negative pressure wound therapy that are used on open wounds. Intended for twice-daily application by a provider to high-risk contact points, DuraDerma augments existing protocols rather than replacing them, improving their efficacy. As a preventive rather than reactive solution, DuraDerma is designed to be the first product labeled to prevent pressure injury progression. The company manufactures medical-grade silk fibroin from raw cocoon to finished product, leveraging the material's decades of regulated clinical use in sutures, dressings, resorbable scaffolds, and drug delivery.
Target Audience
Primary customers are healthcare providers and institutions managing bedridden, immobilized patients, including hospitals and advanced wound care centers that treat hospital-acquired pressure injuries.
Features
- Topical gel formulated with medical-grade silk fibroin to strengthen intact skin
- Cleared as a Class I 510(k) liquid bandage and skin protectant
- Acts preventatively on intact skin, distinct from dressings and NPWT used on open wounds
- Designed for twice-daily provider application to high-risk contact points in bedridden, immobilized patients
- Augments standard of care protocols to improve efficacy without replacing existing treatments
- Targets reduction of risk for both pressure injury formation and progression of early-stage injuries
- Gen 2.0 next-generation formulation in development as a Class II De Novo product, positioned to be the first cleared to reduce pressure injury formation and progression