FDA Announces Record Rate of Novel Device Approvals in 2018

In its return from the federal government shutdown on Monday, the US Food and Drug Administration (FDA) shared news that it had reached a record high of novel device approvals in 2018.

The 2018 final total of 106 devices—approved under Premarket Approval (PMA), panel track supplement PMA, de novo, Humanitarian Device Exemption (HDE), and breakthrough 510(k) pathways—topped last year’s previous high of 98 approved devices. Since 2014, the FDA has approved a new highest annual total of novel devices each year.

Among its novel approvals last year, the FDA also cleared 9 breakthrough designation devices. In a statement announcing the record rate, Commissioner Scott Gottlieb, MD, and Director of the Center for Devices and Radiological Health Jeff Shuren, MD, highlighted a series of innovative devices to receive approval under the administration’s “efficient, risk-based approach to total product life-cycle regulation.”

The highlighted novel devices shared by Gottlieb and Shuren included, among others:

The pair praised the robust innovation in newly-approved devices, as well as the FDA’s commitment to ensuring their safety and benefit for patients.

“Our success in providing patients with new treatments and diagnostics, and more options for effective health care, are not coming at the expense of the robust non-clinical and clinical science on which we rely to make our regulatory decisions,” they said in the statement. He noted the administration’s efforts to strengthen the average applicants’ clinical assessments and their providence of real-world data has led to a more efficient post-market process.

Read more of this MD Magazine article by Kevin Kunzmann by clicking here.

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