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

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

Latest FDA clearance: Nov 2024. Active since 2012.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Straumann USA, Lls as regulatory consultant.