Medical Device Manufacturer · US , Andover , MA

Straumann USA, LLC - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 2012

Total

Cleared

Denied

Straumann USA, LLC has 24 FDA 510(k) cleared medical devices. Based in Andover, US.

Latest FDA clearance: Nov 2024. Active since 2012.

Browse the FDA 510(k) cleared devices submitted by Straumann USA, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Straumann USA, LLC

3 devices

1-3 of 3