Lares Research, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220873Perceptive electric dental motor and control unitDecember 15, 2022
K220874Smooth Drive contra angle and straight handpiecesNovember 7, 2022
K141221LARES ULTRALITE PROSTYLE HIGH-SPEED DENTAL HANDPIECES, LARES EURO PROSTYLE HIGH-SPEED DENTAL HANDPIEOctober 28, 2014
K031540APEX ELECTRIC HANDPIECE SYSTEMJune 30, 2003
K011960LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS POCKETPRO OR POCKETPRO S4)December 21, 2001
K983524LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS PEIOLASE FOR LASERENAP)April 1, 1999
K961163LARES RESEARCH AS-1 LOWSPEED HANDPIECEApril 23, 1996
K905543LARES APOLLO CS/CP/CMarch 11, 1991
K905542LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMSMarch 11, 1991
K905541LARES 757 WORKHORSE HIGHSPEED HANDPIECEMarch 7, 1991