The Straumann Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Straumann Co. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
The Straumann Co. has 14 FDA 510(k) cleared dental devices. Based in Cambridge, US.
Historical record: 14 cleared submissions from 1992 to 2004.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Straumann Co.
14 devices
Cleared
Jul 23, 2004
STRAUMANN TEMPORARY COPING
Dental
88d
Cleared
May 03, 2004
STRAUMANN GRANULES
Dental
53d
Cleared
Apr 30, 2004
THE STRAUMANN ORTHO IMPLANT SYSTEM
Dental
66d
Cleared
Dec 29, 1999
MODUS SAGITTAL SPLIT PLATE
Dental
44d
Cleared
Aug 15, 1996
PLASTIC PROTECTION HEALING CAPS
Dental
84d
Cleared
Jun 18, 1996
TITANIUM HEALING CAPS
Dental
125d
Cleared
Mar 15, 1996
ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES
Dental
120d
Cleared
Jan 23, 1996
MEMFIX
Dental
60d
Cleared
Jun 14, 1995
ITI ANGLED ABUTMENT
Dental
449d
Cleared
Mar 24, 1995
ITI TRANSVERSAL SCREWING SYSTEM
Dental
235d
Cleared
Apr 26, 1994
ITI DISTANCE SYSTEM
Dental
368d
Cleared
Dec 15, 1992
BONE MARROW BIOPSY SYSTEM
General & Plastic Surgery
134d
Cleared
Jul 15, 1992
PRE-STERILIZED ITI DENTAL IMPLANTS
Dental
138d
Cleared
Apr 21, 1992
HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM
Dental
70d