Europe’s Largest OEM Clear Aligner Manufacturer is now in the USA
K Line Europe, the leading OEM Clear Aligners manufacturer in Europe, has recently received FDA registration to introduce its highly popular K Clear.
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K Line Europe, the leading OEM Clear Aligners manufacturer in Europe, has recently received FDA registration to introduce its highly popular K Clear.
The U.S. Food and Drug Administration has provided an at-a-glance summary of news from around the agency: On Monday, the FDA informed consumers.
Vivos Therapeutics, Inc. (the “Company” or “Vivos”) (NASDAQ: VVOS), a medical technology company focused on developing and commercializing innovative diagnostic and treatment modalities.
The US Food and Drug Administration (FDA) is revoking the emergency use authorizations (EUAs) of all disposable respirators that have not been approved.
Overjet has received 510(k) clearance from the Food and Drug Administration (FDA) for its Dental Assist software as a medical device system, which.
The Food and Drug Administration (FDA) has designated Viome’s proprietary mRNA analysis technology, combined with its next generation artificial intelligence (AI) platform, a.
There are three kinds of people in the world—those who understand mathematics, and those who don’t. This joke, which a buddy of mine.
The ADA has joined a coalition of 79 organizations asking the US Food and Drug Administration (FDA) to ban menthol and other non-tobacco.
When Dr. Édouard Lanoiselée met a patient who needed an old amalgam inlay restoration changed with a tooth color restoration, the typical process.
The US Food and Drug Administration (FDA) has created a pair of downloadable infographics about the use of dental amalgam among high-risk patients..