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BioWorld - Monday, June 1, 2026
Home » Topics » Medical technology, Regulatory

Medical technology, Regulatory
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Stephen Hahn, nominee for FDA commissioner

Hahn just a Senate vote away from becoming the FDA’s next commissioner

Dec. 3, 2019
By Mari Serebrov
With today’s 18-5 vote in the Senate Health, Education, Labor and Pensions (HELP) Committee to send Stephen Hahn’s nomination to the full U.S. Senate, the oncologist who currently serves as chief medical officer at the MD Anderson Cancer Center is just a step away from being confirmed as the next FDA commissioner.
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Ear illustration

FDA gives thumbs up to Cochlear’s implantable bone conduction hearing system

Dec. 3, 2019
By Tamra Sami
The U.S. FDA has cleared Cochlear Ltd.’s newest cochlear implant, the Osia 2 system, an active implantable bone conduction hearing system. Unlike Cochlear’s traditional implant, the Osia implant bypasses damaged parts of the ear and sends sound vibrations directly to the cochlea.
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Regulatory front for Dec. 3, 2019

Dec. 3, 2019
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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U.S. flag, stethoscope

Stakeholders press CMS to allow repeat testing in do-over of NGS coverage memo

Dec. 2, 2019
By Mark McCarty
The Medicare coverage memo for next-generation DNA sequencing (NGS) was reopened to allow for NGS testing for other than late-stage cancers, but stakeholders are urging the U.S. Centers for Medicare and Medicaid Services (CMS) to allow repeat testing, another change that would considerably boost utilization.
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Regulatory front for Dec. 2, 2019

Dec. 2, 2019
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Regulatory front for Nov. 27, 2019

Nov. 27, 2019
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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U.S. Capitol building

FDA grappling with Cures impact on software regs as Cures 2.0 unveiled

Nov. 26, 2019
By Mark McCarty
The U.S. FDA has engaged in an overhaul of its software policies in the wake of the mandates spelled out by the 21st Century Cures Act. However, those policies are still a work in progress, as a recent FDA webinar made clear. The FDA won’t have long to put those policies into place as the U.S. House of Representatives is considering a follow-on to the Cures Act, dubbed Cures 2.0, which will impose yet more changes on the agency’s approach to software regulation.
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Doctor looking in child's ear

FDA gives green light to Tusker Medical’s ear tube delivery system

Nov. 26, 2019
By Meg Bryant
Menlo Park, Calif.-based startup Tusker Medical Inc. has received U.S. FDA approval to market its breakthrough-designated system for inserting tympanostomy tubes into the eardrum to treat recurrent ear infections. The Tubes Under Local Anesthesia (Tula) system is the first delivery system for tympanostomy tubes, commonly known as ear tubes, that can be performed in young children under local anesthesia in a doctor’s office. The Tula system consists of the ionic anesthetic Tymbion, Tusker Medical tympanostomy tubes and several devices for inserting the anesthetic and tubes into the ear drum. A low-level electrical charge delivers the anesthesia to the eardrum prior to tube placement, allowing for quick and needle-free numbing of the tympanic membrane.
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Regulatory front for Nov. 26, 2019

Nov. 26, 2019
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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FDA names EtO challenge program participants, tweaks PMA supplement

Nov. 25, 2019
By Mark McCarty
The FDA has posted the names of the companies that will take part in the ethylene oxide (EtO) challenge in response to the recent state action against EtO device sterilization sites, but the agency also has opened a pilot program for a streamlined notification process for changes to sterilization that should be faster and leaner than the usual PMA supplement.
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