Resin dental material BioMed Flex 80A

for anatomical modelsfor 3D printingmodeling

Overview
BioMed Flex 80A Resin is a firm, flexible, translucent medical elastomer formulated for biocompatible 3D-printed parts that require durable skin contact and short-term mucosal contact. Intended for production of patient-specific flexible devices and firm anatomical models. Print with SLA technology at recommended settings.

Key benefits

• Firm yet flexible elastomeric behavior (Shore 80A) enabling deformation and recovery for functional parts.
• Translucent appearance for clear anatomical references and visual inspection.
• Manufactured and tested to medical quality standards (ISO 13485, FDA registration, EU MDR / CE where applicable).
• Biocompatibility testing: ISO 10993 series and USP Class VI for the intended contact scenarios.

Compatibility

• Compatible Build Platforms: Form 4 Build Platform, Form 4 Flex Build Platform, Form 3 Build Platform, Form 3 Build Platform 2, Form 3 Stainless Steel Build Platform, Form 3L Build Platform, Form 3L Build Platform 2L, Form 4L Build Platform, Form 4L Flex Build Platform.
• Compatible Tanks: Form 4 Resin Tank, Form 4L Resin Tank, Form 3 Resin Tank V2.1, Form 3L Resin Tank V3.
• Compatible Printers: Form 4B, Form 4BL, Form 3B, Form 3BL.
• Print Technology: SLA (minimum layer thickness 50 micron).
• Categories: Elastomeric; Medical.
• Color / Appearance: Translucent.

Applications

• Patient-specific flexible medical devices and components requiring prolonged skin contact or short-term mucosal contact.
• Firm, translucent tissue and anatomical models for surgical planning and intraoperative reference.
• Small-batch and mass-personalization workflows where molding is impractical.

Post-processing
Post-processing is required to achieve biocompatible performance: remove uncured resin by thorough alcohol washing and follow the material manufacturing guide/Instructions for Use (IFU) for validated post-cure parameters. Adhere to the specified washing, drying, and post-curing conditions in the IFU before clinical use.

Certifications & Manufacturing
Manufactured in an FDA-registered facility under an ISO 13485-certified Quality Management System. Material testing includes ISO 10993 series and USP Class VI where applicable. Medical device resins are produced following relevant regulatory processes and CE marking per EU MDR when applicable.

Technical specifications

• Ultimate Tensile Strength: 7.2 MPa
• Stress at 50% Elongation: 2.6 MPa
• Stress at 100% Elongation: 4.5 MPa
• Elongation at Break: 135%
• Tear Strength: 22.0 kN/m
• Shore Hardness: 80 A
• Compression Set (70°C for 22 hours): 5.3%
• Minimum Layer Thickness: 50 micron
• Print Technology: SLA
• Biocompatibility: Skin contact (>30 days); Mucosal membrane contact (<24 hours); ISO 10993 and USP Class VI tested
• Color: Translucent