An error has occurred while submitting. Please try again later...
Your form was submitted successfully
The 3M™ Prevena™ Incision Management System is intended to manage the environment of surgical incisions and surrounding intact skin in patients at risk for developing post-operative complications, such as infection, by maintaining a closed environment via the application of negative pressure therapy to the incision.
It is indicated by FDA to help reduce superficial surgical site infections in patients at high-risk for post-operative complications in Class I and Class II wounds.*
Prevena Therapy Mechanism of Action flyer (PDF, 300.31 KB)
Prevena Therapy portfolio brochure (PDF, 2.14 MB)
Prevena Therapy Mechanism of Action video
*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 myKCI.com.
PRM with Prevena Therapy provides healthcare professionals with an evidence-based, standardized approach that helps to advance the standard of care for closed incision negative pressure therapy (ciNPT). This intuitive, actionable model is grounded in level 1, 2 and 3 clinical evidence to help support you through procedural and patient risk stratification.
Prevena Therapy for Patients
This helpful website explains the 3M™ Prevena™ Incision management system, as well as what to expect while a patient is using Prevena Therapy. Patients can find instructions, information on caring for the system, as well as frequently asked questions.
VuMedi
Find Prevena Therapy information on VuMedi, an online video education platform dedicated to delivering comprehensive healthcare professional education from leading institutions and practitioners.
Negative Pressure Therapy (NPT) product page
View product details and resources for 3M NPT kits, dressings, devices and accessories.
3M™ Prevena Restor™ Therapy product page
See how Prevena Restor Therapy can help elevate your patients' postoperative outcomes by helping protect the surgical site and optimizing the healing environment.
View a comprehensive list of conferences we will be attending and information about upcoming medical education events.
3M has partnered with Sharps® Compliance, Inc. for the safe and environmentally friendly disposal of your 3M single-patient use, negative pressure therapy units, at no cost to you.
Contact a 3M representative for information or to request a demonstration.
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 risk for post-operative infections, aid in reducing the incidence of superficial surgical site infection in Class I and II wounds.
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 myKCI.com.
NOTE: Applicable therapy units include Prevena™ 125 and Prevena™ Plus 125 Therapy Unit 7 Day.
The indication statement does not apply to the Prevena Plus 125 Therapy Unit (14-day) that comes with the 3M™ Prevena Restor™ System Kits (see Prevena Restor indications for use).
The 3M™ Prevena Restor™ Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudate via the application of negative pressure wound therapy.
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.