RENASYS WOUND+ Dressing Kit with AIRLOCK Technology
K-Number: K251826 · 2025-09-11
Device Summary
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. The listed applicant is Smith & Nephew Medical, Ltd.. The 510(k) number is K251826.
When did RENASYS WOUND+ Dressing Kit with AIRLOCK Technology receive FDA 510(k) clearance?
RENASYS WOUND+ Dressing Kit with AIRLOCK Technology received FDA 510(k) clearance on 2025-09-11, under 510(k) number K251826.
Who is the listed applicant for RENASYS WOUND+ Dressing Kit with AIRLOCK Technology?
The FDA 510(k) record lists Smith & Nephew Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Smith & Nephew Medical, Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OMP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.