Millennium Dental Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Millennium Dental Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PerioLase Nd:YAG Pulsed Dental Laser System
5
Total
5
Cleared
0
Denied
Millennium Dental Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Castro Valley, US.
Historical record: 5 cleared submissions from 2001 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Millennium Dental Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Millennium Dental Technologies, Inc.
5 devices
Cleared
Jul 12, 2019
PerioLase Nd:YAG Pulsed Dental Laser System
General & Plastic Surgery
263d
Cleared
Mar 15, 2016
PerioLase Nd:YAG Pulsed Dental Laser System
General & Plastic Surgery
260d
Cleared
Jul 26, 2004
PERIOLASE ND:YAG DENTAL LASER SYSTEM
General & Plastic Surgery
550d
Cleared
Mar 27, 2002
PERIOLASE ND:YAG DENTAL LASER SYSTEM
General & Plastic Surgery
90d
Cleared
Nov 27, 2001
PERIOLASE ND:YAG DENTAL LASER SYSTEM
General & Plastic Surgery
258d