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FDA 510(k) clearance

By Jessica Hagen | 02:19 pm | March 19, 2025
The company has secured 510(k) clearance for its Apple Watch-powered seizure monitoring platform, expanding the role of wearables in epilepsy care.
By Jessica Hagen | 12:20 pm | March 27, 2023
The company's product, Prism, uses neurofeedback to help PTSD patients learn to control their emotional response.
By Mallory Hackett | 03:14 pm | August 02, 2021
This marks the fourth clearance for Volpara’s breast health platform since its original authorization back in 2010.  
By Mallory Hackett | 03:31 pm | July 27, 2021
The system is designated to be used by clinicians to monitor patients at home or in the healthcare setting.   
By Mallory Hackett | 02:10 pm | May 11, 2021
The company has developed a line of products targeting the mammography space to enable early and accurate breast cancer detection.   
By Mallory Hackett | 12:58 pm | May 10, 2021
The system was cleared for use among individuals 12 years old and up with Type 1 or Type 2 diabetes on multiple-dose injection therapy.  
By Mallory Hackett | 12:46 pm | January 25, 2021
Nerivio is a wireless, noninvasive remote electrical-stimulation wearable that is worn on the upper arm at the onset of a migraine.   
By Mallory Hackett | 03:51 pm | July 28, 2020
Using this tool can help radiologists speed up the diagnosis process and reduce missed cases, according to the company.
By Dave Muoio | 03:31 pm | April 02, 2019
The Loop System continuously collects and analyzes health data to warn providers of potential deterioration. The company says it has already inked a deal with a major health system.
By Dave Muoio | 04:39 pm | November 08, 2018
The AI tool helps clinicians prioritize patients in need of immediate diagnosis, but does not render these decisions on its own.