By Actuated Medical, Inc. Actuated Medical, a leading innovator in medical device technologies, proudly announces the receipt of FDA 510(k) clearance for its groundbreaking GripTract-GI™ Endoscopic Tissue Manipulator (GripTract-GI).
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By Hoth Intelligence Hoth Intelligence, a health care augmented reality software company, announced today that the U.S.
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| By Successful Human Factors™ SHF 2.0 Framework as Practical Solution to Drive Continuous Improvement
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| By Spa Sciences Devices not cleared by the FDA are being sold in the USA! Buying non-FDA cleared devices can cause injury. Spa Sciences launches LEXI after receiving FDA clearance for effective treatment.
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By American Conference Institute Join the "who's who" of the FDA Bar virtually from March 22-23, 2023.
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By Actuated Medical, Inc. The FDA has issued a 510(k) Clearance for the Shippert Tech Intraosseous Safety Sheath. As a Critical Care physician, Dr. Brian Shippert has seen colleagues accidentally stick themselves while removing interosseous (IO) needles from patients.
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| By Incubator LLC New App Automates the USA FDA "Prior Notice" and Customs Forms Process
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By Quality Smart Solutions Quality Smart Solutions, a global consulting regulatory compliance firm headquartered near Toronto, is excited to announce it'll be hosting an online webinar – Public Registration is open now!
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