Smith & Nephew Medical Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Smith & Nephew Medical Limited - FDA 510(k) Cleared Devices
Recent clearances: BIOBRANE Temporary Wound Dressing, ALLEVYN Ag+ Border Antimicrobial Silicone Gel Adhesive Composite Hydrocellular Foam Dressing, ALLEVYN Ag+ Border Sacrum Antimicrobial Silicone Gel Adhesive Composite Hydrocellular Foam Dressing, ALLEVYN Ag+ Surgical Antimicrobial Silicone Gel Adhesive Composite Hydrocellular Foam Dressing, VERSAJET Hydrosurgery System (III)
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.