Evonik Industries, Jenacell, Jena
Biomaterials for Wound Care & Medical Devices

Advanced biomaterial solutions for chronic wound care

Every year, millions of people worldwide need medical care for burn injuries and chronic wounds. Evonik develops and manufactures the biomaterials that make this care possible – from bioresorbable polymers supplied as raw materials to medical device manufacturers, to our own market-approved wound dressings made from biosynthetic cellulose. As a partner to medical device companies, we combine decades of materials expertise with regulatory experience – from initial formulation all the way to commercial-scale manufacturing under GMP and ISO 13485.

Wound Care: An Underserved Market with Growing Demand

The numbers show why better material solutions in wound care are urgently needed:

  • An estimated 11 million people worldwide sustain burn injuries requiring medical attention every year – more than 30,000 new cases every day.
  • Burns cause an estimated 180,000 to 250,000 deaths annually, the vast majority in low- and middle-income countries.
  • The global chronic wound care market is valued at around USD 15 billion (2025) and continues to grow steadily, driven by diabetes, vascular disease, and an aging population.
  • Roughly 19% to 34% of all people with diabetes develop a diabetic foot ulcer over the course of their disease — one of the most common causes of chronic, hard-to-heal wounds.
  • Venous leg ulcers affect an estimated 1 to 5 percent of the elderly population in Europe and North America.

These trends are increasing the pressure on hospitals, care facilities, and medical device manufacturers to offer more effective, better-tolerated, and more cost-efficient wound care solutions. This is exactly where Evonik's materials expertise comes in.

Our Portfolio: From Raw Material to Certified Medical Device

Evonik covers the full value chain of bio-based wound care materials — as a raw material partner for our customers' own formulations, and as a manufacturer of our own clinically proven medical devices.

Bioresorbable Polymers for Medical Device Development

Our portfolio of RESOMER® bioresorbable polymers — including poly-L-lactic acid (PLLA), polycaprolactone (PCL), and polydioxanone (PDO) — forms the material science foundation for numerous modern medical devices. Manufacturers use our materials to develop implants, wound dressings, suture materials, and other resorbable applications where controlled degradation in the body plays a central role.

This portfolio is complemented by VECOLLAN®, our recombinant, non-animal-derived collagen platform. As a biomimetic material, VECOLLAN® actively interacts with surrounding tissue and can support wound healing, while offering the purity, consistency, and scalability required for regulated medical devices. A key advantage for developers: VECOLLAN® can be combined with our bioresorbable polymers. This enables combination products that pair the mechanical stability and defined degradation time of resorbable polymers with the biological activity of a collagen-based material — for applications that require both structural integrity and active tissue regeneration.

Biosynthetic Cellulose: As a Raw Material and as a Finished Medical Device

Through our subsidiary JeNaCell GmbH, part of Evonik since 2021, we produce biosynthetic cellulose — a nature-identical, high-purity material with more than 95 percent water content, manufactured through a fermentation process in Germany. This material platform is available to manufacturers in two forms: as a raw material under the brand biocellic® for custom product development and private-label solutions, and as a finished, MDR-certified medical device under the brand epicite®. All three epicite® product lines are certified according to MDR standards, and together they demonstrate the clinical applicability of the underlying material technology' across a range of several indications

epicite® BALANCE — A hydro-active wound dressing for chronic and complex wounds such as lower extremity ulcers, diabetic foot ulcer, and pressure ulcers. Supports autolytic wound cleansing and reactivates stalled healing processes.

epicite® RESCUE — A wound dressing for burn care and acute wounds. Clinically shown to cool and relieve pain, with dwell times on the wound of up to 14 days — reducing dressing changes, anesthesia procedures, and hospital stays.*

epicite® CALM — Medical-grade and sterile post-treatment care following laser, light, and energy-based aesthetic procedures, as well as surgical interventions such as facelifts or blepharoplasty.

All three product lines are built on the same underlying principle: a finely branched, hydrophilic cellulose fiber network that creates an ideally moist wound environment, absorbs exudate in a controlled way, and supports the body's own healing process — without additives, fragrances, or preservatives.

Highlights for wound care

RESOMER®

VECOLLAN®

Related documents

Recombinant collagen platform for life sciences

Want to learn more about epicite®? Visit our dedicated websites for health care professionals:

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epicite® BALANCE

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epicite® CALM

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epicite® RESCUE

Partner with Evonik to Accelerate Wound Care Innovation

Whether you're developing next-generation wound dressings, bioactive therapies, implantable devices or regenerative medicine solutions, Evonik offers biomaterial expertise across the development lifecycle.

Our capabilities include:

  • Biomaterial selection and formulation support
  • Prototype development
  • Process scale-up
  • Quality and regulatory support
  • Commercial manufacturing
  • Clinical and market experience through our own medical device portfolio

Looking for New Materials or Product Solutions?

"Whether you need bioresorbable raw materials for your own product development or biosynthetic cellulose for an innovative wound care concept — our team supports you from your first technical question through to commercial implementation."

 

Mandy Roovers-Wiermans
Business Development Manager Medical Device Solutions

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Frequently asked questions (FAQ)

Evonik offers a broad portfolio of RESOMER® bioresorbable polymers as well as VECOLLAN®, a recombinant collagen platform, and biosynthetic cellulose under the biocellic® platform. All materials are designed for use in regulated medical devices and implant applications.

Yes. VECOLLAN® in particular can be combined with bioresorbable polymers to develop products that support both mechanical stability and active tissue regeneration.

Both. In addition to raw materials for our customers' own product development, Evonik also manufactures its own market-approved wound dressings made from biosynthetic cellulose under the epicite® brand — proof of the clinical maturity of our material technology.

Both. Under the epicite® brand, we sell biosynthetic cellulose as a finished, market-approved medical device. For manufacturers who want to develop their own formulations or private-label solutions, we also offer the same material technology as a raw material platform under the brand biocellic®. This allows customers to bring their own, individually developed wound care or medical device products to market, built on our biosynthetic cellulose.

Our production platforms scale from small laboratory samples to full commercial-volume manufacturing, allowing formulations to be tested and optimized before larger quantities are ordered.

All materials are manufactured under ISO 13485 quality systems, as required for use in medical devices intended for human application.

Yes. We support customers with the technical documentation and material characterization data needed for regulatory submissions. 

Our biomaterials are used in wound care, resorbable implants, suture material development, and medical aesthetics, among other fields. Depending on the desired degradation behavior and mechanical requirements, our team will recommend the right material or material combination together with you.

The process typically starts with an initial technical discussion, often under NDA, to understand your formulation and product goals. This is followed by sample development and joint testing ahead of commercialization.


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