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BioWorld - Friday, December 26, 2025
Home » Topics » FDA, BioWorld MedTech

FDA, BioWorld MedTech
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Medtronic Minimed insulin pump

Medtronic recalls select Minimed insulin delivery systems

Oct. 4, 2024
By Holland Johnson
Medtronic plc reported a voluntary recall of certain insulin pumps after customers said a single drop, bump, or physical impact could shorten their battery life.
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Sen. Cassidy: Time for US FDA to reclaim its Orange Book duties

Oct. 2, 2024
By Mari Serebrov
It’s well past time for the U.S. FDA to end its silence on what device patents can be listed in the Orange Book as part of a drug-device combination product, Sen. Bill Cassidy (R-La.) said in an Oct. 1 letter that took FDA Commissioner Robert Califf to task for letting the FTC do the FDA’s job.
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Setpoint medical neurstim device

Setpoint receives IDE for neuromodulation therapy for MS

Oct. 2, 2024
By Annette Boyle
Setpoint Medical Inc. received U.S. FDA investigational device exemption approval to initiate a study of its neuroimmune modulation platform in people living with relapsing-remitting multiple sclerosis. Setpoint plans to launch the 60-person trial in 2025 to evaluate the use of its implantable neurostimulation device to slow or reverse the nerve damage characteristic of multiple sclerosis.
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U.S. Capitol building

Two House members seek answers in Jeff Shuren controversy

Oct. 1, 2024
By Mark McCarty
The controversy over conflicts of interest for Jeff Shuren, formerly the director of the U.S. FDA’s device center, reached Capitol Hill and may lead to an executive branch investigation into the matter.
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AI-generated illustration of heart and metabolic impact

Pi-Cardia receives FDA greenlight for transcatheter leaflet splitter

Sep. 30, 2024
By Shani Alexander
The Pi-Cardia Ltd. Shortcut — the catheter-based, leaflet modification solution for treating heart valves — received U.S. FDA clearance. The device was granted breakthrough device designation from the regulatory agency and is designed to split bioprosthetic aortic valve leaflets in patients undergoing valve-in-valve transcatheter aortic valve replacement (TAVR) procedures who are at risk of coronary obstruction.
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Ribbons of digital data

FDA’s AI glossary includes ‘AI performance monitoring’

Sep. 30, 2024
By Mark McCarty
The question of how to define artificial intelligence (AI) for medical product usage was answered by the FDA, which recently offered an AI glossary.
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Illustration of calcified artery, heart

FDA approves GE Healthcare’s Flyrcado for CAD diagnosis

Sep. 30, 2024
By Annette Boyle
GE Healthcare Technologies Inc. received U.S. FDA approval for its novel radiotracer, Flyrcado (flurpiridaz F-18), for use in the diagnosis of myocardial ischemia or infarction in patients with known or suspected coronary artery disease.
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Dental X-ray

FDA takes a bite out of confusion with four new dental guidances

Sep. 30, 2024
By Mark McCarty
The U.S. FDA has guidances on the books for dental products, but the it unleashed a quartet of guidances – ceramics and cements used in dental procedure – for dental products on the final Friday of September 2024. The agency also issued a guidance without comment – unusual for the FDA – for the well-known, terror-striking pneumatic dental hand tool.
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U.S. Capitol building

US Congress avoids government shutdown, extends voucher program

Sep. 26, 2024
By Mari Serebrov
Both chambers of the U.S. Congress put aside their election year politicking Sept. 25 long enough to pass a continuing resolution that will keep the government running at its current funding level through Dec. 20.
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U.S. Capitol building

US Congress avoids government shutdown, extends voucher program

Sep. 26, 2024
By Mari Serebrov
Both chambers of the U.S. Congress put aside their election year politicking Sept. 25 long enough to pass a continuing resolution that will keep the government running at its current funding level through Dec. 20. The spending bill is now awaiting President Joe Biden’s signature.
Read More
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