Regulation

Casana's Heart Seat
By  Emily Olsen 11:48 am May 3, 2023
Casana, maker of a health monitoring smart toilet seat, announced this week it had received its first FDA 510(k) clearance. The startup's Heart Seat received the agency green light for monitoring heart rate and oxygen saturation in adults at least 22 years and older who weigh 90 to 350 pounds. Casana said the battery-powered seat can run for several years without recharging, sending health data...
Moderator David Gray and Jodi Daniel
By  Emily Olsen 02:52 pm April 19, 2023
After years of slow movement advancing telehealth, remote patient monitoring and other digital health technologies, the landscape changed rapidly during the COVID-19 pandemic, said Jodi Daniel, managing director of Crowell Health Solutions.  At HIMSS23, Daniel, who previously served as the founding director of the Office of Policy in the Office of the National Coordinator for Health Information...
A gavel and a stethoscope.
By  Emily Olsen 01:09 pm April 12, 2023
A federal jury found three former executives of health tech company Outcome Health guilty of multiple counts of fraud on Tuesday.  Rishi Shah, cofounder and former CEO, Shradha Agarwal, former president, and Brad Purdy, former chief operating officer and chief financial officer, were convicted for their roles in a $1 billion scheme that defrauded investors and clients, largely pharma companies....
Healthcare provider looking at x-ray images on a tablet
By  Jessica Hagen 10:40 am April 10, 2023
Butterfly Network, maker of a handheld, smartphone-connected ultrasound system, received FDA 510(k) clearance for its Auto B-line Counter that leverages AI to help providers determine if a patient has abnormal lung function by measuring B-lines.  B-lines on an ultrasound appear as bright lines and can be associated with various pulmonary conditions, such as chronic obstructive pulmonary disease...
Person looking at a wearable on their wrist
By  Jessica Hagen 11:18 am March 24, 2023
Digital health technology company NeuroRPM has received FDA 510(k) clearance for its AI-enabled remote monitoring app that utilizes an Apple Watch to track common Parkinson's symptoms such as bradykinesia, tremor and dyskinesia. Bradykinesia is slowness of movement, and dyskinesia is involuntary or erratic movements.  The Washington D.C.-based company's algorithms are embedded in the Apple Watch...
A person wearing a mask walking by a CVS pharmacy
By  Emily Olsen 11:17 am March 24, 2023
Sen. Elizabeth Warren (D-Mass.) is urging the Federal Trade Commission to scrutinize CVS Health's planned acquisition of Medicare-focused primary care provider Oak Street Health. In a letter to FTC Chair Lina Khan and Commissioners Alvaro Bedoya and Rebecca Slaughter, the progressive senator wrote the deal could lower quality of care and hike costs.  She also pointed to other acquisitions – ...
Adult and child talking to a provider through a video chat
By  Emily Olsen 12:26 pm March 15, 2023
Virtual primary care company TytoCare received FDA 510(k) clearance for clinical decision support software that analyzes lung sounds for possible wheezing.  Tyto Insights for Wheeze Detection uses TytoCare's stethoscope to evaluate lung sounds and identify recordings that suggest wheezing in adults and children ages 2 and older. It prompts a clinician when wheezing is suspected.  The software...
A person using a laptop.
By  Emily Olsen 10:13 am March 3, 2023
The Federal Trade Commission has started cracking down on digital health companies for allegedly sharing consumers' health data for advertising purposes.  Last month, the agency said GoodRx had shared personal health information with third parties like Google and Facebook. The company, best known for its drug-cost transparency tools, agreed to pay a $1.5 million fine to settle the case, but...
A person talking to a provider through a video chat on a tablet.
By  Emily Olsen 12:58 pm March 2, 2023
The Federal Trade Commission has fined online therapy company BetterHelp $7.8 million for allegedly sharing consumer data with third parties like Facebook and Snapchat for advertising purposes. The proposed order – the second recent action by the FTC regarding data sharing by a digital health company – would also ban BetterHelp from disclosing health data for advertising. The agency said this is...
An adult and child wearing the Nerivio device.
By  Emily Olsen 10:16 am March 1, 2023
Prescription digital therapeutic developer Theranica announced it has received FDA 510(k) clearance to use its Nerivio device for migraine prevention in patients 12 and older.  The wearable is worn around the upper arm and controlled with a smartphone. It delivers electrical pulses to stimulate small peripheral nerves, which aims to trigger a conditioned pain modulation response to alleviate...