Sulzer Calcitek, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sulzer Calcitek, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Sulzer Calcitek, Inc. has 9 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 9 cleared submissions from 1997 to 2001. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sulzer Calcitek, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sulzer Calcitek, Inc.
9 devices
Cleared
Jan 19, 2001
SPLINE DENTAL IMPLANT SYSTEM
Dental
10d
Cleared
Jun 21, 2000
TEMPORARY GINGIVAL CUFF AND IMPRESSION POST AND IMPLANT ANALOG
Dental
8d
Cleared
Jun 16, 1999
REMOVABLE CUFF ABUTMENT
Dental
177d
Cleared
Sep 22, 1998
SPLINE DENTAL IMPLANT SYSTEM-TEMPORARY ABUTMENT
Dental
83d
Cleared
Jul 30, 1998
SPLINE DENTAL IMPLANT SYSTEM - SPLINE XI IMPLANT
Dental
90d
Cleared
Nov 20, 1997
VARIABLE PARALLEL PIN
Dental
64d
Cleared
Jun 23, 1997
EDOSSEOUS DENTAL IMPLANT
Dental
160d
Cleared
Jun 23, 1997
SPLINE ENGAGING SHOULDERED ABUTMENT SYSTEM
Dental
112d
Cleared
Feb 25, 1997
THREADLOC DENTAL IMPLANT SYSTEMS
Dental
90d