Medical Device Manufacturer · US , Andover , MA

Straumann USA (On Behalf of Institut Straumann Ag) - FDA 510(k) Clear...

2 submissions · 2 cleared · Since 2007
2
Total
2
Cleared
0
Denied

Straumann USA (On Behalf of Institut Straumann Ag) has 2 FDA 510(k) cleared medical devices. Based in Andover, US.

Historical record: 2 cleared submissions from 2007 to 2010. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Straumann USA (On Behalf of Institut Straumann Ag) Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Straumann USA (On Behalf of Institut Straumann Ag)
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