Sulzer Dental, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sulzer Dental, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Sulzer Dental, Inc. has 9 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 9 cleared submissions from 2001 to 2002. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sulzer Dental, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sulzer Dental, Inc.
9 devices
Cleared
Nov 13, 2002
HEX-LOCK TEMPORARY ABUTMENT
Dental
338d
Cleared
Mar 20, 2002
SULZER DENTAL CERAMIC SYSTEM-HEXLOCK
Dental
90d
Cleared
Mar 19, 2002
SULZER DENTAL CERAMIC SYSTEM-SPLINE
Dental
88d
Cleared
Jan 18, 2002
3.75MM AND 5.0MM SPLINE TWIST IMPLANT
Dental
88d
Cleared
Nov 19, 2001
SCREW VENT IMPLANT
Dental
53d
Cleared
Sep 06, 2001
3.25MM SPLINE TWIST IMPLANT
Dental
66d
Cleared
Jun 25, 2001
ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM
Dental
63d
Cleared
May 21, 2001
SCREW-VENT DENTAL IMPLANT SYSTEM
Dental
46d
Cleared
May 15, 2001
TAPER-LOCK DENTAL IMPLANT SYSTEM
Dental
40d