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	Nova Biomedical New Generation StatStrip Glucose Hospital Meter Obtains FDA 510k Clearance By Nova Biomedical Nova Biomedical announces the U.S. launch of our New Generation StatStrip Glucose Hospital Meter System.
Actuated Medical Celebrates FDA 510(k) Clearance for their GripTract-GI™ Endoscopic Tissue Manipulator, Enhancing Complex Colonoscopy Visualization 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).
Augmented Reality Software Company, Hoth Intelligence Receives First FDA 510k Approval By Hoth Intelligence Hoth Intelligence, a health care augmented reality software company, announced today that the U.S.
	Research Urges Standardization of FDA's Human Factors Engineering Practices Within the Medical Device Industry By Successful Human Factors™ SHF 2.0 Framework as Practical Solution to Drive Continuous Improvement
	# 1 Facial Skin Device Brand Spa Sciences Receives FDA Clearance for its IPL Device LEXI for Home-Use Hair Removal 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.
ACI's FDA Boot Camp Will Feature FDORA Updates this March By American Conference Institute Join the "who's who" of the FDA Bar virtually from March 22-23, 2023.
Shippert Tech, LLC Intraosseous Safety Sheath Receives FDA 510(k) Clearance 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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