Poly-Med partners with medical device innovators to design, develop, and manufacture custom absorbable medical implants, supporting programs from early concept through production.
With integrated expertise across absorbable biomaterials, development, manufacturing, analytical testing, we help transform complex device ideas into tangible, high-performance product opportunities.
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Absorbable medical device development requires more than standard contract manufacturing. Material selection, degradation behavior, processing conditions, device performance, testing, validation, and quality requirements all need to work together.
Poly-Med brings these elements into one integrated development and manufacturing environment, helping partners move from feasibility and prototype work toward validated production pathways.
Poly-Med’s absorbable and synthetic biomaterials can be converted into a range of implantable medical device applications across specialized markets.
Absorbable and synthetic biomaterials for applications such as hernia meshes, plastic surgery meshes, tissue scaffolds, and barrier applications.
Materials and components for applications such as load-bearing sutures, tendon meshes and bands, bone scaffolds, and related implantable device concepts.
Nanofibrous tissue scaffold technologies and barrier applications designed to support advanced wound and burn care needs.
Raw absorbable and synthetic polymers that can support implantable device development and processing needs.
Whether you are exploring feasibility, refining a prototype, preparing for process validation, or planning for production, Poly-Med can support the technical and manufacturing needs of absorbable medical device programs.
Support for feasibility, proof-of-concept work, and early material or process exploration.
Support for prototype characterization, process definition, manufacturing instructions, and development activities that prepare a product for production transfer.
Support for production planning, process validation, repeatability, and ongoing manufacturing needs.
Poly-Med’s Design Assets can help customers move from early concept exploration toward more defined product development pathways. These assets provide a starting point for teams evaluating absorbable biomaterials, device architectures, processing options, and performance requirements.
By combining Poly-Med’s existing design knowledge with custom development, manufacturing, analytical testing, and quality support, customers can reduce early uncertainty and build from proven technical foundations.
Hernia Mesh
Plastic Surgery Mesh
Void Filler
Wound Matrix / Skin Substitute
Wound Matrix Powder
Tendon Mesh
Tendon Band
Orthopedic Suture
Bone Scaffold
Bone Screw & Anchor
Poly-Med’s design and development process is structured to support the full idea-to-market evolution of bioresorbable medical device programs. Each stage helps define, test, refine, and prepare the product and process for future production needs.
1
Feasibility
Early laboratory work and R&D activities help establish proof of concept, define early boundaries, and begin discussions around material, component, and process specifications.
2
Design & Development
Functional prototypes are characterized, manufacturing processes are identified, and initial manufacturing instructions or work instructions are prepared for traceability.
3
Transfer to Production / Process Validation
Development work continues into manufacturing transfer, with activities focused on process validation, repeatability, client requirements, and process capability.
Poly-Med’s CDMO model brings together the core services required to support absorbable and implantable medical device programs, from early development through manufacturing and quality-controlled production.
Absorbable medical device programs often require coordination across material development, processing, component manufacturing, testing, validation, and production. When these steps are split across multiple vendors, complexity can increase quickly.
Poly-Med’s vertically integrated model helps streamline that process by bringing absorbable polymer expertise, manufacturing capabilities, analytical testing, and quality systems into a connected development and production pathway.
Poly-Med supports absorbable medical device development through a broad range of material, processing, and manufacturing capabilities designed for complex implantable device applications.
Absorbable polymer materials designed to support next-generation medical device development.
Monofilament fibers, multifilament yarns, films, and other inputs for biomedical textile and device applications.
Fibrous articles and medical textiles built around absorbable polymer performance and device requirements.
Nanofibrous scaffold technologies that can be tailored to support the healing process.
Absorbable implant architectures created through filament-based and resin-based approaches.
Poly-Med provides integrated support for absorbable and implantable medical device programs, including design and development, vertically integrated manufacturing, analytical testing, and quality systems.
Poly-Med supports absorbable and implantable medical device programs across markets such as soft tissue reinforcement and scaffold implants, orthopedics and craniomaxillofacial implants, advanced wound and burn tissue scaffolds, and absorbable biomaterial applications.
Yes. Poly-Med’s development process begins with feasibility and proof-of-concept work, helping define material, component, and process needs before moving into design, development, and production planning.
Yes. Poly-Med’s pathway includes transfer to production and process validation, supported by ongoing manufacturing capabilities tailored to client requirements and program needs.
Poly-Med’s vertically integrated model brings together absorbable polymer expertise, processing, manufacturing, testing, and quality systems to support a more connected development and production pathway.
Yes. Poly-Med provides in-house analytical characterization and polymer testing to support absorbable material evaluation, development decisions, custom test methods, and release testing needs.
Poly-Med is FDA registered and ISO 13485 compliant, with quality-controlled methodologies supporting validation, production, audits, testing protocols, and release requirements.
Connect with Poly-Med to discuss your development, manufacturing, testing, or commercialization needs.
We provide an adaptable approach to customer needs for any medical application. How can we help you?
Interested in learning about Poly-Med's bioresorbable polymer portfolio and processing capabilities? Complete this form to receive the catalog.
We provide an adaptable approach to customer needs for any medical application. How can we help you?
Please provide your name and email to view our ISO Certificate.
Please provide your name and email to view our Max-Prene® Polymer Data Sheet.
We provide an adaptable approach to customer needs for any medical application. How can we help you?
We provide an adaptable approach to customer needs for any medical application. How can we help you?
Please provide your name and email to view our Photoset® 311 Resin Data Sheet.
Please provide your name and email to view our Dioxaprene® Polymer Data Sheet.
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Please provide your name and email to view our Lactoprene® Polymer Series Data Sheets.
Please provide your name and email to view our Aquaprene® Polymer Data Sheet.
Please provide your name and email to view our Lactoflex® 7415 3DP Filament Data Sheet.
Please provide your name and email to view our Dioxaprene® 100M 3DP Filament Data Sheet.
Please provide your name and email to view our Lactoprene® 100M 3DP Filament Data Sheet.
Please provide your name and email to view our Strataprene® 5525 3DP Filament Data Sheet.
Please provide your name and email to view our Caproprene® 100M 3DP Filament Data Sheet.
Please provide your name and email to view our Strataprene® Polymer Series Data Sheets.
Please provide your name and email to view our ISO Certificate.