Calcitek, Inc. is one of 14582 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Calcitek, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SPLINE X ENDOSSEOUS DENTAL IMPLANT SYSTEM, SPLINE DENTAL IMPLANT SYSTEMS, 5.0MM SPLINE ENDOSSEOUS DENTAL IMPLANT SYSTEMS
21
Total
21
Cleared
0
Denied
Calcitek, Inc. has 21 FDA 510(k) cleared dental devices. Based in Walker, US.
Historical record: 21 cleared submissions from 1984 to 1997.
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 - Calcitek, Inc.
21 devices
Cleared
Feb 10, 1997
SPLINE X ENDOSSEOUS DENTAL IMPLANT SYSTEM
Dental
224d
Cleared
Aug 29, 1996
SPLINE DENTAL IMPLANT SYSTEMS
Dental
90d
Cleared
Mar 08, 1996
5.0MM SPLINE ENDOSSEOUS DENTAL IMPLANT SYSTEMS
Dental
88d
Cleared
Feb 08, 1996
INTEGRAL V BIOINTEGRATED DENTAL IMPLANT SYSTEM
Dental
563d
Cleared
Feb 08, 1996
CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS
Dental
37d
Cleared
Nov 15, 1995
INTEGRAL VII 4.9MM BIOINTEGRATED DENTAL IMPLANT SYSTEM
Dental
322d
Cleared
Nov 15, 1995
INTEGRAL VIII BIOINTEGRATED DENTAL IMPLANT SYSTEM
Dental
320d
Cleared
Oct 04, 1995
INTEGRAL VII 3.25MM BIOINTEGRATED DENTAL IMPLANT SYSTEM
Dental
280d
Cleared
Sep 21, 1995
INTEGRAL IV BIOINTEGRATED DENTAL IMPLANT SYSTEM
Dental
447d
Cleared
May 16, 1995
INTEGRAL VI BIOINTEGRATED DENTAL IMPLANT SYSTEM
Dental
256d
Cleared
May 05, 1995
INTEGRAL OMNILOC DENTAL IMPLANT WITH INTERFACE RING
Dental
399d
Cleared
Aug 01, 1994
INTEGRAL III BIOINTEGRATED DENTAL IMPLANT SYSTEM
Dental
637d