Light Age, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
5
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K113115EPICARE YAGApril 3, 2012
K110370Q-CLEARSeptember 15, 2011
K091625EPICARE-DUO LASER SYSTEMNovember 3, 2009
K032991LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPXSeptember 14, 2004
K033259LIGHT AGE Q-CLEAR LASER, MODEL 701-1101February 25, 2004
K983977LIGHT AGE EPICARE ALEXANDRITE LASERJanuary 7, 1999
K980131ALEX TA2 ERASERFebruary 17, 1998