510(k) K251826

RENASYS WOUND+ Dressing Kit with AIRLOCK Technology by Smith & Nephew Medical, Ltd. — Product Code OMP

K251826 is an FDA 510(k) premarket notification submitted by Smith & Nephew Medical, Ltd. for the device "RENASYS WOUND+ Dressing Kit with AIRLOCK Technology". The FDA issued a decision of Substantially Equivalent on September 11, 2025. The device falls under product code OMP (Negative Pressure Wound Therapy Powered Suction Pump), a Class II device regulated under 21 CFR 878.4780. Smith & Nephew Medical, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 2025
Date Received
June 13, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Negative Pressure Wound Therapy Powered Suction Pump
Device Class
Class II
Regulation Number
878.4780
Review Panel
SU
Submission Type

For wound management via application of continual or intermittent negative pressure to the wound for removal of fluids, including wound exudate, irrigation fluids, and infectious materials. The Device is indicated for management of chronic, acute, traumatic, subacute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts.