FDA Expands Warning About Methanol Hand Sanitizers
The US Food and Drug Administration (FDA) continues to warn consumers and healthcare professionals that they should not be using certain alcohol-based hand.
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The US Food and Drug Administration (FDA) continues to warn consumers and healthcare professionals that they should not be using certain alcohol-based hand.
The Food and Drug Administration (FDA) has issued a warning letter to Dr. Jason Korkus, DDS, and Sonrisa Family Dental, doing business as.
LaunchPad Medical has received $1.8 million from the Michigan-Pittsburgh-Wyss Regenerative Medicine Resource Center to improve the translation of promising tissue engineering and regenerative.
As experts agree that widespread testing is necessary to identify who has and doesn’t have the COVID-19 coronavirus, the ADA is asking the Department.
Biolase is partnering with MEK-ICS Co Ltd, a Korean intensive care unit (ICU) equipment manufacturer, to supply MEK-ICS’s MTV1000 ICU-grade portable ventilator through Biolase’s FDA-registered.
As COVID-19 cases continue to rise, the World Health Organization (WHO) and the Centers for Disease Control and Prevention (CDC) are warning about.
The US Food and Drug Administration (FDA) has cleared Nobio’s Infinix Flowable Composite and Bulk Fill Flow Composite for marketing. According to the company,.
Soligenix is actively enrolling patients in a Phase 3 multinational, double-blind, placebo-controlled clinical trial of SGX942, or dusquetide, for the treatment of oral mucositis.
LaunchPad Medical says that it has successfully enrolled half of the 20 patients approved by the US Food and Drug Administration (FDA) for its.
The ADA has announced a new interim policy on vaping, calling for a total ban on vaping products that aren’t approved by the.