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

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

2 devices

1-2 of 2

Cleared Dec 16, 2010

STRAUMANN MEMBRAGEL

Cleared Sep 26, 2007

P.004 ABUTMENTS

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 28, 2026