... Barotz Dental is now one of only two dental practices in Denver offering LANAP (Laser Assisted New Attachment Procedure). This is the only laser gum treatment protocol that is patented and FDA approved for new attachment of gum and bone tissue around teet...

... The petition was filed in U.S. Bankruptcy Court in Austin. The company has struggled since September, when the U.S. Food and Drug Administration rejected its application to market Advexin. Introgen submitted the application in June as a long-awaited...

...required warnings and disclosures, according to an advocacy group. Wednesday, the Prescription Project petitioned the Food and Drug Administration to update its advertising rules specifically to address such Internet marketing. As the Web has grown as a...

... This press release contains forward-looking statements, and such statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements involve risks and uncertainties that could cause actual ...

...Ring), an annuloplasty ring used in heart valve repair, has not been approved and/or cleared for marketing by the Food and Drug Administration (FDA)," he wrote. The surgeon, Dr. Patrick McCarthy, appears to have invented the device and receives royalty payments...

...of paper work would have discovered, but a deliberate adulteration with an ingredient that would pass ordinary quality control drug inspection by the well known and respected American and European (and Japanese) drug companies. So pass a law, hire some inspectors,...

...to make plastics and fertilizers, to falsely raise the protein counts of diluted dairy products. Last month, the Food and Drug Administration said that imports of a variety of Chinese products that contain milk, including candy, snacks, baker products and...

...advertising their products on YouTube, the Prescription Project said in citizen petitions filed today with the Food and Drug Administration (FDA). The non-profit industry watchdog group is asking the FDA to enforce its rules and require Abbott Laboratories...

...The European Agency for the Evaluation of Medicinal Products receives 75% of its funding in this way, 43% of the US Food and Drug Administration (FDA) budget is similarly derived, and the UK's Medicines and Healthcare Products Regulatory Agency is completely...

...update or revise any forward-looking statements for any reason. In the United States, NanoKnife has been cleared by the Food and Drug Administration ("FDA?) for use in the surgical ablation of soft tissue. This document may discuss the use of the NanoKnife...