Dental implantology has seen remarkable advancements over the past decades, improving patient outcomes and expanding treatment possibilities. However, with innovation comes the critical responsibility of ensuring implant safety, biocompatibility, and quality. Regulatory frameworks such as the US Food and Drug Administration (FDA) and the European Medical Device Regulation (MDR) establish stringent requirements for implant manufacturers, influencing how implants are designed, tested, and marketed. In this landscape, CleanImplant has emerged as a vital mediator, bridging the gap between patient care, scientific research, and industry collaboration.
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