KCI's Prevena Becomes First FDA-Cleared Negative Pressure Wound-Closure Device

The US FDA granted KCI's de novo request for the Prevena incision management system, making it the first negative pressure device cleared for reducing superficial surgical site infections in patients at high risk.

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• Source: shutterstock.com

The US Food and Drug Administration has granted KCI Medical Services’ de novo request for its Prevena incision management system, making it the first disposable negative pressure system designed specifically for the management of closed surgical incisions available in the US.

Prevena is a closed-incision negative-pressure therapy that removes fluid away from the surgical incision via the application of -125 mmHg...

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