Medical Device Manufacturer · GB , Hull

Smith & Nephew Medical, Ltd. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2016

Recent clearances: RENASYS DYNAFLOW Kit (66807741), RENASYS EDGE (66803126), RENASYS WOUND+ Dressing Kit with AIRLOCK Technology

9
Total
9
Cleared
0
Denied

Smith & Nephew Medical, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Hull, GB.

Latest FDA clearance: Sep 2026. Active since 2016. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Smith & Nephew Medical, Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Smith & Nephew, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Smith & Nephew Medical, Ltd.

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