The World of Health & Medicine News

FDA scrutiny of WHOOP signals challenges for niche wearable device makers

FDA scrutiny of WHOOP signals challenges for niche wearable device makers

Niche fitness-tracking firms such as WHOOP are coming under increased regulatory scrutiny as technological advances blur the lines between wearable and medical devices, exposing them to higher compliance costs ​and hampering their competitive advantage.

Although the U.S. Food and Drug Administration regulates certain health-focused tools in wearable devices such as smartwatches, many ‌companies have until now used a “regulatory gray zone” to bundle apps such as blood pressure monitors under advanced wellness features, without formal approvals.

However, the regulator has started to crack the ‌whip by making it clear that features such as blood pressure monitoring may be used by consumers to manage underlying health conditions and therefore would need its approval.

STRICTER NORMS TO RAISE COSTS

Stricter norms for wearable makers would mean increased investments, including higher spending on clinical and cybersecurity testing, upgraded quality-management systems, hardware or software redesigns and third-party audits.

This can potentially raise R&D costs and slow down launches for niche players such as WHOOP in a fast-growing $90 billion wearables ⁠market.

“What was once a land rush of health tech ‌innovation is now seeing the regulatory sheriff ride into town,” said Michael Ashley Schulman, chief investment officer at Running Point Capital.

Companies must either limit functionality or embrace regulation, which could slow development and strain budgets, Schulman said, adding that ‍features like blood-oxygen estimation and heart-rhythm detection have pushed startups closer to what they considered to be the boundary of medical claims.

WHOOP has already come under the FDA’s firing line.

The agency in July warned WHOOP that its blood-pressure insights feature made the company’s wearable product look more like a medical device as it estimated systolic ​and diastolic values used in diagnosing hypertension.

WHOOP, when contacted by Reuters, said it disagrees with the FDA’s stance.

“We continue to stand by Blood ‌Pressure Insights as a wellness feature designed to help members understand how blood pressure interacts with sleep, stress, exercise, and overall performance – not to diagnose or treat any medical condition,” a WHOOP spokesperson said.

In contrast, Apple recently sought FDA clearance for its smartwatch’s recent hypertension notification feature, which it says does not diagnose or manage hypertension.

spot_img

Explore more

spot_img

GSK enters lung cancer drug market with early FDA nod for...

GSK enters lung cancer drug market with early FDA nod for Jideytro GSK (GSK.L), opens new tab said on Wednesday the U.S. FDA approved its drug ​to...

Working from home could be harming your health, warns Chris Whitty

Working from home could be harming your health, warns Chris Whitty England’s chief medical officer has issued a warning about the health dangers of prolonged sitting, coinciding...

Popular sugar substitutes linked to faster brain aging

Popular sugar substitutes linked to faster brain aging Several popular sugar substitutes may not be as harmless as they seem. Adults who consumed the most...

 The Best Time to Eat Peaches for Energy, According to a...

The Best Time to Eat Peaches for Energy, According to a Dietitian Peaches are a juicy, naturally sweet, nutritious, and refreshing fruit. While there’s no...

FDA approves at-home starter dose of Eisai-Biogen Alzheimer’s drug

FDA approves at-home starter dose of Eisai-Biogen Alzheimer's drug The U.S. FDA on Monday approved an at-home starting dose of Eisai's (4523.T), opens new tab and Biogen's (BIIB.O),...

The One Healthy Food That Might be Spiking Your ‘Bad’ Cholesterol

The One Healthy Food That Might be Spiking Your 'Bad' Cholesterol Coconut oil has enjoyed a long run as a wellness favorite. It's been blended...

US FDA approves Vertex’s gene therapy for sickle cell disease in...

US FDA approves Vertex's gene therapy for sickle cell disease in children as young as two The U.S. Food and Drug Administration approved expanded use...

FDA clears Orca’s blood cancer therapy to reduce stem cell transplant...

FDA clears Orca's blood cancer therapy to reduce stem cell transplant complications The U.S. Food and Drug Administration said on ​Tuesday it has approved Orca...