Bioresorbable polymers for dermal fillers and biostimulators
Highlights for aesthetic dermatology
Suitable Products
Why partner with Evonik for medical aesthetic applications?
- Broad portfolio of bioresorbable and biocompatible materials
- Unique RESOMER® Powder Platform with customization capability
- Strong application, formulation, and regulatory support
- GMP and ISO 13485 manufacturing
- Decades of experience supporting global medical device manufacturers
Frequently asked questions (FAQ)
Evonik supplies high-purity bioresorbable polymer powders and microgranules used by medical device manufacturers to develop aesthetic injectable products. RESOMER® materials are raw materials, not finished medical devices — formulation, regulatory approval, and commercialization remain the responsibility of the device manufacturer.
PLLA, PDLLA, PCL, and PDO grades are commonly used in biostimulation products for medical aesthetics. Within the Evonik portfolio, these are available across the RESOMER® L-series, R-series, X-series, and C-series.
RESOMER® powders are suspended or otherwise processed into injectable filler systems. Once formulated into a finished product, the bioresorbable polymer contributes to application-specific performance characteristics depending on product design and intended clinical use.
Material characteristics, including particle size, can influence suspension behavior, injectability, and other formulation attributes. Evonik's solvent-free micronization platform enables manufacturers to select particle characteristics that support specific development objectives.
Yes. Beyond our standard powder grades, the RESOMER® Powder Select platform offers customization options to support specific formulation and product-development requirements.
Yes. We support customers with the technical and quality documentation needed for regulatory submissions, including material characterization data and biocompatibility testing references aligned with ISO 10993.
Yes. Our micronization platform scales from small laboratory batches up to full commercial volumes, so formulations can be trialed and optimized with limited material before scaling into larger orders.
Yes. Evonik operates production facilities and application centers for medical-grade biomaterials in Darmstadt (Germany), Birmingham (USA), and Shanghai (China), all manufactured under the same GMP and ISO 13485 quality systems — supporting a seamless path from early-stage testing to commercial-scale supply.
Our team typically begins with an initial technical discussion under NDA to understand your formulation goals, followed by sample development and joint testing.