Thrilled to announce that hipro obtain the 510(k) certification issued by the US FDA, which is a milestone achievement marking the company's major breakthrough in the field of medical devices. This certification is not only an international authoritative endorsement of the safety and efficacy of Hobbes' products, but also paves the way for the company's innovative products to enter the U.S. market, which greatly enhances its competitiveness in the global market.
The United States Food and Drug Administration（FDA） is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of food supply, cosmetics, and products that emit radiation.
For Hipro, this certification will greatly facilitate our business expansion globally, especially in the U.S. market. As one of the world's largest medical device markets, the United States has high entry barriers and strict regulations. However, once successfully entered, it will bring huge business opportunities and brand influence to enterprises. With this certification, Hipro's products will be more likely to gain the trust of American medical institutions and consumers, thereby accelerating the expansion of market share.
