Smith & Nephew Inc., Endoscopy Division

Smith & Nephew Inc., Endoscopy Division holds 8 FDA 510(k) medical device clearances, first cleared 2007, most recent 2013, with 37 FDA device recalls on record.

Top product codes for Smith & Nephew Inc., Endoscopy Division

FDA recalls by Smith & Nephew Inc., Endoscopy Division

10 most recent of 37

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by Smith & Nephew Inc., Endoscopy Division

Data sourced from openFDA. This site is unofficial and independent of the FDA.