American Dental Technologies, Inc. is one of 21541 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
Recent clearances: DIOLASE 980 D LASER SYSTEM, PULSEMASTER ERBIUM DENTAL LASER SYSTEM, GULLIVER AND CLASSE A
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.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
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