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How New Executive Orders May Affect FDA’s Medical Device Operations
Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...
Pharmabiz1mon
CDSCO seeks industry comment on updated classification list of four medical devices categories
The drug regulator has sought the industry to submit their comments ... as Class A comprising low risk devices, Class B for low moderate risk devices, Class C for moderate high risk products, and ...
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FDA tags Sentec/Percussionaire’s breathing circuit recall as Class I
The US Food and Drug Administration (FDA) has tagged a recall of breathing circuits manufactured by Sentec/Percussionaire as ...
2025 Medical Device Cybersecurity Trends: What Will Shape The Industry?
What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
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FDA labels recall of discontinued Olympus endoscope accessory as Class I
In recent years, Olympus has recalled other devices because of patient safety risks and ... In its Class I recall notice, the agency’s most serious classification, the FDA said patient exposure to a ...