Advanced Bone and Tissue Fusing Implants for Superior Surgical Outcomes
- 30% Less Post-Op Swelling: DMI implants reduce the body’s acute inflammatory response, allowing for a significantly faster healing process.
- Reduced Risk of Infections and Rejections: DMI implants actively inhibit biofilm formation, reducing the potential for infections and rejections.
The Next Generation of Facial a Reconstruction
Bio-Integration
Our implants actively promote tissue regeneration, working with your body’s natural healing processes rather than simply replacing tissue.
Structural Integrity
Mimics natural bone architecture while providing the strength and stability essential for successful reconstruction.
Cell Proliferation and Mineralization 28 Days

Biocompatibility Testing
ISO 10993-5:2009 cytotoxicity, ISO 10993-10:2021 irritation and sensitization protocols completed successfully.
Systemic Safety
ISO 10993-11:2017 systemic toxicity and ISO 10993-23:2021 irritation testing demonstrate non-toxic profile.
Cell Proliferation and Mineralization 21 Days
Multiple Sterilization
Compatible with gamma radiation, e-beam, and ethylene oxide sterilization methods for flexible manufacturing workflows.

REACH Compliant
- Full compliance with European Chemical Regulation (EC1907/2006) ensuring safety and environmental responsibility.
ISO 10993 Certified
Complete biocompatibility testing, including cytotoxicity, sensitization, irritation, and systemic toxicity protocols.
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Trusted by Leading Institutions
DMI partners with premier surgical organizations committed to advancing patient care and surgical excellence.
Surgeons can learn more about partnering with DMI, and our sterilization protocol outlines how these implants are prepared for surgery. Curious about the material itself? See why we never manufacture standard PEEK, or browse our Implant FAQs.




- Our implants are designed and manufactured in the USA under rigorous quality control standards, with ISO 13485 certification ensuring consistent excellence.