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How to Make Sure You're Getting the Real Deal with BOTOX Cosmetic
⏲ 1:43 👁 960K
Is My Product A Medical Device
⏲ 24 minutes 👁 5.7K
How is My Medical Device Classified?
⏲ 16 minutes 18 seconds 👁 5.5K
NeuroOne – The Medical Device Company That Has Created A Product That Could Monitor And Treat At The Same Time
⏲ 10:0 👁 230K
Medical Device Regulations FDA Approval
⏲ 9 minutes 28 seconds 👁 15.5K
FDA 101 for Medical Devices
⏲ 57 minutes 47 seconds 👁 17.6K
E. coli Outbreak Linked to Organic Walnuts Under Investigation
⏲ 0:50 👁 25.9M
FDA Regulation of Medical Devices and Software Apps
⏲ 15 minutes 54 seconds 👁 3.5K
Overview of the USA FDA Classification Process
⏲ 6 minutes 50 seconds 👁 8.3K
FDA Commissioner Robert Califf Testifies Before The Senate Appropriations Committee
⏲ 1:17:50 👁 65K
FDA Product Regulations Part 1 of 7
⏲ 28 minutes 23 seconds 👁 4.7K
Medical Devices 101: An Entry Level Overview of the FDA
⏲ 49 minutes 8 seconds 👁 468
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_how-to-make-sure-you39re-getting-the-real-deal-with-botox-cosmetic.webp "Over the last two decades, BOTOX Cosmetic has become a household name--making it the number one selling product of its kind, the one approved to temporarily make moderate to severe forehead lines, crow's feet lines and frown lines look better in adults. But people may forget, it is a medical procedure. Many people are interested in learning more about getting treated and there is only one BOTOX Cosmetic, but how do you know you're getting the real BOTOX Cosmetic? This FDA approved one-of-a-kind formulation through its manufacturing process and scientific rigor can temporarily improve the look of three areas--moderate to severe frown lines, crow's feet lines, and forehead lines in adults. Board-certified dermatologist, Dr. Michelle Henry teamed up with Allergan Aesthetics, an AbbVie company-the makers of BOTOX Cosmetic, and the only authorized suppliers of BOTOX Cosmetic in the US-to show us how to ensure product safety, quality, and efficacy. What happens in many cases is people use the word 'Botox' ubiquitously, not specifically for BOTOX Cosmetic. The FDA has stated BOTOX Cosmetic is 'not interchangeable,' which means that its safety and effectiveness cannot be claimed by any other product. There are no substitutes for BOTOX Cosmetic. Potential flags to look out for: significantly discounted product may indicate it's not the real deal, supplier claims their product is 'equivalent to BOTOX Cosmetic' or 'approved in another country,' and lastly, if it feels too good to be true, it may be. It's extremely important to only go to medical professionals who are licensed and trained to provide aesthetic treatments both for safety and to help you achieve your desired outcomes. To find a licensed provider near you, who is purchasing BOTOX Cosmetic from Allergan Aesthetics, visit Alle.com .")
_is-my-product-a-medical-device.webp "U.S. Food and Drug Administration")
_how-is-my-medical-device-classified.webp "U.S. Food and Drug Administration")
_neuroone-the-medical-device-company-that-has-created-a-product-that-could-monitor-and-treat-at-the-same-time.webp "Dave Rosa, President & CEO of NeuroOne, was recently a guest on Benzinga's All-Access.<br/><br/>NeuroOne is a medical device company that designs and manufactures high-definition, minimally invasive thin film electrodes used for intracranial monitoring and ablation. The devices diagnose and treat several neurological conditions like epilepsy and Parkinson's Disease. They are implanted inside the skull to record brain activity. That data helps surgeons better locate and remove the brain tissue causing issues without impacting the rest of the brain. <br/><br/>The company also has a minimally invasive device that can be implanted in the spine, aiming to treat back pain.")
_medical-device-regulations-fda-approval.webp "The BME Life")
_fda-101-for-medical-devices.webp "Registrar Corp")
_e-coli-outbreak-linked-to-organic-walnuts-under-investigation.webp "The CDC and FDA are investigating an E. coli outbreak associated with organic walnuts sold in food co-ops and natural food stores. With 12 reported cases and seven hospitalizations in California and Washington, concerns are rising. Veuer’s Maria Mercedes Galuppo has the story.")
_fda-regulation-of-medical-devices-and-software-apps.webp "Fast Forward Medical Innovation – Commercialization Education")
_overview-of-the-usa-fda-classification-process.webp "Emergo by UL")
_fda-commissioner-robert-califf-testifies-before-the-senate-appropriations-committee.webp "On Wednesday, FDA Commissioner Dr. Robert Califf testified before the Senate Appropriations Committee on the FDA FY2025 budget request. <br/><br/>Fuel your success with Forbes. Gain unlimited access to premium journalism, including breaking news, groundbreaking in-depth reported stories, daily digests and more. Plus, members get a front-row seat at members-only events with leading thinkers and doers, access to premium video that can help you get ahead, an ad-light experience, early access to select products including NFT drops and more:<br/><br/>https://account.forbes.com/membership/?utm_source=youtube&utm_medium=display&utm_campaign=growth_non-sub_paid_subscribe_ytdescript<br/><br/><br/>Stay Connected<br/>Forbes on Facebook: http://fb.com/forbes<br/>Forbes Video on Twitter: http://www.twitter.com/forbes<br/>Forbes Video on Instagram: http://instagram.com/forbes<br/>More From Forbes:http://forbes.com")
_fda-product-regulations-part-1-of-7.webp "NIH VideoCast")
_medical-devices-101-an-entry-level-overview-of-the-fda.webp "leanRAQA")
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