American Dental Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Dental Technologies, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
American Dental Technologies, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Carlos, US.
Historical record: 8 cleared submissions from 1995 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Dental Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Dental Technologies, Inc.
8 devices
Cleared
Apr 15, 2003
DIOLASE 980 D LASER SYSTEM
General & Plastic Surgery
176d
Cleared
Oct 04, 2001
PULSEMASTER ERBIUM DENTAL LASER SYSTEM
General & Plastic Surgery
87d
Cleared
Aug 13, 2001
GULLIVER AND CLASSE A
Dental
28d
Cleared
May 13, 1999
PULSEMASTER DENTAL LASER SYSTEM
General & Plastic Surgery
147d
Cleared
Sep 19, 1997
PULSEMASTER 1000 ST DENTAL LASER SYSTEM
General & Plastic Surgery
88d
Cleared
Mar 10, 1997
PULSEMASTER
General & Plastic Surgery
342d
Cleared
Jun 03, 1996
PULSEMASTER
General & Plastic Surgery
74d
Cleared
Aug 10, 1995
PLASMA ARC CURING SYSTEM
Dental
84d