Smith & Nephew Medical Limited has 20 FDA 510(k) cleared general & plastic surgery devices. Based in Hull, GB.

Latest FDA clearance: Dec 2024. Active since 2016.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Smith & Nephew, Smith and Nephew and Smith Nephew Medical Limited.

FDA 510(k) Regulatory Record - Smith & Nephew Medical Limited

20 devices
1-12 of 20
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