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FDA 510(k)

RENASYS WOUND+ Dressing Kit with AIRLOCK Technology

K-Number: K251826 · 2025-09-11

Decision Date2025-09-11
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RENASYS WOUND+ Dressing Kit with AIRLOCK Technology is a medical device manufactured by Smith & Nephew Medical, Ltd.. It received FDA 510(k) clearance on 2025-09-11 under approval number K251826. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENASYS WOUND+ Dressing Kit with AIRLOCK Technology?

RENASYS WOUND+ Dressing Kit with AIRLOCK Technology is a medical device that received FDA 510(k) clearance on 2025-09-11. It is manufactured by Smith & Nephew Medical, Ltd.. The 510(k) number is K251826.

When was RENASYS WOUND+ Dressing Kit with AIRLOCK Technology approved by the FDA?

RENASYS WOUND+ Dressing Kit with AIRLOCK Technology received FDA 510(k) clearance on 2025-09-11, under approval number K251826.

What company makes RENASYS WOUND+ Dressing Kit with AIRLOCK Technology?

RENASYS WOUND+ Dressing Kit with AIRLOCK Technology is manufactured by Smith & Nephew Medical, Ltd..

What is the FDA product code for RENASYS WOUND+ Dressing Kit with AIRLOCK Technology?

The FDA product code for RENASYS WOUND+ Dressing Kit with AIRLOCK Technology is OMP.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.