Aug. 13, 2025
| Today’s news and insights for medtech leaders
Hospitals are being advised to stop using the filters after serious injuries were reported related to the problem, the FDA said in a recall notice.
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The appointment comes weeks after the company received 510(k) clearance for its wearable heart monitor.
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New limits to the program could force hospitals to slash capital spending while bracing for millions of newly uninsured patients.
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Abbott and Boston Scientific are among the investors in SetPoint, whose neurostimulation device gained FDA approval last month.
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The company’s stock rose in its first two days on public markets, closing on Monday up almost 58% over the IPO price amid investor enthusiasm.
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