, /PRNewswire/ — The global periodontal disease treatment market is projected to reach USD 3.63 billion by 2030 from USD 2.58 billion in 2024, growing at a CAGR of 5.9% during the forecast period 2024-2030. In all the regions, the regulatory environment of the treatment of periodontal disease is focused primarily on safety and efficacy considerations concerning therapeutic products and procedures. In the United States, dental devices-including dental implants, lasers, and others-are regulated by the Food and Drug Administration (FDA), which validates that they meet rigid standards of safety before marketing. Such drugs, again, which include antibiotics and antiseptics, the FDA demands clinical evidence to prove the efficacy of such drugs in reducing periodontal pathogens, with secondary inflammation.
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In the European region, the legal system involving drugs is the European Medicines Agency (EMA) and devices under the Medical Device …