Implant Innovations International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Implant Innovations International, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Implant Innovations International, Inc. has 18 FDA 510(k) cleared dental devices. Based in West Palm Beach, US.
Historical record: 18 cleared submissions from 1987 to 1995.
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 - Implant Innovations International, Inc.
18 devices
Cleared
Mar 13, 1995
3I STANDARD THREADED/SELF-TAPPING THREADED IMPLANTS MODIFICATION
Dental
486d
Cleared
May 27, 1994
IMPLANT INNOVATION PRE-ANGLED ABUTMENT SYSTEM
Dental
389d
Cleared
Oct 21, 1991
IMPLARETTE
Dental
192d
Cleared
Jun 10, 1991
ABUTMENT GLO
Dental
194d
Cleared
May 15, 1991
G-FLOSS & G-FLOSS II
Dental
29d
Cleared
Oct 10, 1989
OVERDENTURE ATTACHMENT
Dental
204d
Cleared
Jun 12, 1989
DRILLING MACHINE W/HANDPIECES & INTERNAL IRRIGA.
Dental
84d
Cleared
May 01, 1989
INSERTION TOOLS
Dental
42d
Cleared
Apr 17, 1989
SURGICAL DRILLS
Dental
28d
Cleared
Apr 17, 1989
TITANIUM FORCEPS
Dental
28d
Cleared
May 11, 1988
INNOVATIVE IMPLANTS AND COVER SCREWS
Dental
184d
Cleared
Mar 02, 1988
NON-ROTATING GOLD CYLINDER AND SCREW
Dental
126d
Cleared
Nov 12, 1987
TITANIUM SUCTION TIP
Dental
15d
Cleared
Jul 31, 1987
TEMPORARY BRIDGE HEAD
Dental
72d
Cleared
Jul 31, 1987
ABUTMENT HEAD POST
Dental
72d
Cleared
Jul 31, 1987
TEMPORARY SCREW
Dental
72d
Cleared
Jul 10, 1987
POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER
Dental
58d
Cleared
Jul 10, 1987
ADBUTMENT CYLINDER AND SCREW
Dental
58d