Straumann Manufacturing, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Straumann Manufacturing, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Straumann Manufacturing, Inc. has 4 FDA 510(k) cleared medical devices. Based in Andover, US.
Historical record: 4 cleared submissions from 2007 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Straumann Manufacturing, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Straumann Manufacturing, Inc.
4 devices
Cleared
Dec 15, 2009
STRAUMANN DENTAL ABUTMENTS
Dental
92d
Cleared
Feb 26, 2009
MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS
Dental
23d
Cleared
Apr 30, 2008
P.004 ABUTMENTS, P.004 TEMPORARY COPINGS, P.004 PROTECTIVE CAPS, P.004...
Dental
90d
Cleared
Sep 20, 2007
P.004 RC TEMPORARY ABUTMENT, P.004 TEMPORARY HEALING ABUTMENT (CAP)
Dental
212d