Medical Device Manufacturer · US , Andover , MA

Smith & Nephew Inc., Endoscopy Division - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2007

Total

Cleared

Denied

Smith & Nephew Inc., Endoscopy Division has 8 FDA 510(k) cleared medical devices. Based in Andover, US.

Historical record: 8 cleared submissions from 2007 to 2013. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Smith & Nephew Inc., Endoscopy Division

8 devices

1-8 of 8