Medtronic's second quarter profits more than doubled — and the company said it expects continued improvement the rest of the year and raised its fiscal guidance.
Medtronic CEO Geoff Martha said that many of the challenges during the pandemic — supply-chain issues and a decline in medical procedures — have been mitigated and that the med-tech market is stabilizing.
At the same time, the company's research and development efforts have further driven growth. The U.S. Food and Drug Administration approved seven new devices, including the MiniMed 780G insulin pump, so far this year.
Those products — and more in the pipeline — will continue to drive increased sales, Martha said as he highlighted the list.
On Friday, the FDA approved Medtronic's Symplicity Spyral, a renal denervation system to treat hypertension. It was a long road for approval between early trials that were not as promising as expected. As late as August, an FDA advisory panel expressed concerns about the device.
"This opens up a multibillion-dollar market opportunity for us," Martha said about the renal denervation business.
Martha called the Aurora EV-ICD, a new implantable defibrillator approved in October, "a game changer."
Martha also pointed to Evolut, a transcatheter aortic valve implantation system approved in Europe in October, as another bright spot for sales growth.