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Tag: Food and Drug Administration (FDA)

FDA Releases Guidance for Cannabis

The U.S. Food and Drug Administration (FDA) has issued final instructions for creating medications derived from cannabis. Including information on the specific differences between...

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Selux Diagnostics secures FDA 510(k) clearance for AST testing NGP System

<!----> The US Food and Drug Administration (FDA) has granted 510(k) clearance to Boston-based biotech startup SeLux Diagnostics’s...

Are Delta-8 THC Sales Hurting the Legal Cannabis Market? How About $2 Billion in Delta-8 THC Sales in the Last 24 Months

Delta-8 THC products have gained significant popularity in recent years, with over $2 billion in sales as an alternative to traditional marijuana. A recent...

Shockwave Medical signs deal to buy Neovasc

<!----> Shockwave Medical has signed a definitive agreement to buy all outstanding shares of Neovasc, a speciality medical...

What Would Happen If the FDA Begins Regulating CBD?

It is so amazing that cannabidiol (CBD) is now mainstream. Around a decade ago, this kind of thing was unthinkable. But because marijuana legalization...

BD launches third-generation total lab automation system

<!----> Becton, Dickinson and Company (BD) has launched the new third-generation BD Kiestra Total Lab Automation System for...

Q4 startup roundup: Cultivated meat’s big moment, plus the rise of bees

This article originally appeared as part of our Food Weekly newsletter. Subscribe to get sustainability food news in your inbox every Thursday. With headline-dominating layoffs, the last...

Medcura Receives Breakthrough Device Designation for its LifeGel™ Absorbable Surgical Hemostat

  COLLEGE PARK, Md., Jan. 12, 2023 /PRNewswire/ -- Medcura, Inc., a medical device company dedicated to transformatively improving the management of surgical...

Neuralink launches patient registry to improve technology

By Maria Merano Posted on January 10, 2023 ...

US FDA grants EUA for BD and CerTest’s PCR test to detect Mpox

<!----> Becton, Dickinson and Company (BD) and CerTest Biotec have announced that their molecular assay for detecting the...

Pristine Surgical’s Summit arthroscope secures FDA 510(k) clearance

<!----> Medical technology manufacturer Pristine Surgical has secured 510(k) clearance for its Summit 4K single-use surgical arthroscope from...

Vivos’ DNA oral appliance gets FDA 510(k) clearance to treat OSA

<!----> Vivos Therapeutics has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its DNA...

Pristine Surgical Receives FDA 510(k) Clearance for Summit™, the World’s First 4K Single-Use Surgical Arthroscope

Designed to Improve Procedure Efficiency, Consistency, and Safety MANCHESTER, N.H.--(BUSINESS WIRE)-- Medical device company Pristine Surgical received 510(k) clearance from the U.S. Food and Drug...

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