Straumann USA, LLC (On Behalf of Institut Straumann Ag) is one of 14040 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Straumann USA, LLC (On Behalf of Institut Straumann Ag) - FDA 510(k) ...
Recent clearances: Straumann BLX Gold Abutments, Straumann Screw Retained Abutments, Straumann PURE Ceramic Implants
3
Total
3
Cleared
0
Denied
Straumann USA, LLC (On Behalf of Institut Straumann Ag) has 3 FDA 510(k) cleared medical devices. Based in Andover, US.
Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Straumann USA, LLC (On Behalf of Institut Straumann Ag) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Straumann USA, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Straumann USA, LLC (On Behalf of Institut Straumann Ag)
3 devices