3M(TM) Prevena(TM) Therapy in use during a surgery

  • Get the clinical evidence.

    3M™ Prevena™ Therapy is the only medical device indicated by FDA to help reduce superficial surgical site infections in high-risk patients with Class I and II wounds.* Click submit and get access to clinical evidence from specific applications that helped support this designation.


    What you’ll receive:

    Orthopedic

    A downloadable summary of six high-evidence orthopedic articles, including key points from two Level I RCTs.


    Cardio, Vascular and Plastic

    Quick links to 4-5 studies focused on Prevena Therapy's use on closed incisions after specific procedures.

    A 3M Prevena Therapy specialist will follow up with you via email.

    *The effectiveness of Prevena Therapy in reducing the incidence of SSIs and seroma in all surgical procedures and populations has not been demonstrated. See full indications for use and limitations at 3M.com.

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  • Submit

3M™ Prevena™ 125 and 3M™ Prevena Plus™ 125 Therapy Units manage the environment of closed surgical incisions and remove fluid away from the surgical incision via the application of -125mmHg continuous negative pressure. When used with legally marketed compatible dressings, Prevena 125 and Prevena Plus 125 Therapy Units are intended to aid in reducing the incidence of seroma; and in patients at high risk for post-operative infections, aid in reducing the incidence of superficial surgical site infection in Class I and Class II wounds.

NOTE: Specific indications, limitations, contraindications, warnings, precautions and safety information exist for these products and therapies. Please consult a clinician and product instructions for use prior to application. Rx only.

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PRA-PM-US-03090 (04/21).

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