Karl Storz Endoscopy

Karl Storz Endoscopy holds 35 FDA 510(k) medical device clearances, first cleared 1995, most recent 2005, with 71 FDA device recalls on record.

Top product codes for Karl Storz Endoscopy

FDA recalls by Karl Storz Endoscopy

10 most recent of 71

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 Karl Storz Endoscopy

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