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BioWorld - Monday, July 6, 2026
Home » Topics » Medical technology, Regulatory

Medical technology, Regulatory
Medical technology, Regulatory RSS Feed RSS

New DOJ interim rule codifies terms of Brand memo

Aug. 27, 2020
By Mark McCarty
The U.S. Department of Justice (DOJ) unveiled two interim final rules intended to deal with enforcement activities in connection with policies enunciated over the past four years, including the so-called Brand memo, which banned federal prosecutors from using federal agency guidance as leverage in prosecutions of private-sector entities.
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8-26-Abbott_BinaxNow_kit

Abbott’s $5 COVID-19 rapid test wins FDA emergency use nod

Aug. 27, 2020
By Meg Bryant
The U.S. FDA has cleared the way for Abbott Laboratories sixth COVID-19 test, a near-patient, point-of-care antigen test that gives results in 15 minutes and can be run without laboratory equipment. The company has priced the Binaxnow COVID-19 Ag Card rapid test at $5 and is offering a complementary mobile app that allows people to display their test results when asked by organizations for verification.
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Regulatory front for Aug. 27, 2020

Aug. 27, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Centers for Medicare & Medicaid Services, FDA, HHS, NICE, Stericycle Expert Solutions.
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8-26-BrainsWay_DeepTMS

FDA clears first brain stimulation device for smoking cessation

Aug. 26, 2020
By Mary Ellen Schneider
The U.S. FDA has given the green light to a new type of treatment to help smokers quit, clearing the way for the first time the use of deep transcranial magnetic stimulation (Deep TMS) for short-term smoking cessation in adults.
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FDA gives green light to Jointechlabs’ MiniTC device

Aug. 26, 2020
By Meg Bryant
Regenerative therapies startup Jointechlabs Inc. has won the U.S. FDA’s nod for its MiniTC point-of-care fat tissue processing device. The 510(k)-cleared product is designed to extract microfat for use in grafts for a variety of indications, including medical aesthetics, plastic surgery, orthobiologics and wound healing.
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SARS-CoV-2 molecular diagnostic

Stenzel mum on LDT question, but says FDA ‘overwhelmed’ with EUA filings

Aug. 26, 2020
By Mark McCarty
A number of controversies have swirled around the U.S. FDA’s handling of the COVID-19 pandemic, including the question of the emergency use authorization (EUA) program for testing. The FDA’s Tim Stenzel said on an Aug. 26 testing town hall that he would not answer questions about the rescission order for FDA regulation of lab-developed tests (LDTs), but also said, “we are simply overwhelmed” with EUA filings for testing.
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Regulatory front for Aug. 26, 2020

Aug. 26, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Centers for Medicare & Medicaid Services, HHS.
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Regulatory actions for Aug. 26, 2020

Aug. 26, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Fluidigm, Inova, Jointechlabs, Natera, Surgentec.
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Regulatory front for Aug. 25, 2020

Aug. 25, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: ASP, Genzyme, Smiths Medical, WLF.
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Regulatory actions for Aug. 25, 2020

Aug. 25, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: B. Braun, Gyroscope, Philips, Sientra.
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