Lares Research, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lares Research, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Lares Research, Inc. has 8 FDA 510(k) cleared medical devices. Based in Chico, US.
Historical record: 8 cleared submissions from 1991 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Lares Research, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lares Research, Inc.
8 devices
Cleared
Oct 28, 2014
LARES ULTRALITE PROSTYLE HIGH-SPEED DENTAL HANDPIECES, LARES EURO PROSTYLE...
Dental
169d
Cleared
Jun 30, 2003
APEX ELECTRIC HANDPIECE SYSTEM
Dental
45d
Cleared
Dec 21, 2001
LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS POCKETPRO OR...
General & Plastic Surgery
182d
Cleared
Apr 01, 1999
LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS PEIOLASE FOR LASERENAP)
General & Plastic Surgery
175d
Cleared
Apr 23, 1996
LARES RESEARCH AS-1 LOWSPEED HANDPIECE
Dental
32d
Cleared
Mar 11, 1991
LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS
Dental
90d
Cleared
Mar 11, 1991
LARES APOLLO CS/CP/C
Dental
90d
Cleared
Mar 07, 1991
LARES 757 WORKHORSE HIGHSPEED HANDPIECE
Dental
86d