Litecure, LLC

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K173067LightForce LTS Model 1000, 1500, 2500, and 4000February 22, 2018
K123014LITECURE THERAPY SYSTEM MODEL LTS-1500March 29, 2013
K123031BWF-5 MEDICAL LASER SERIESDecember 3, 2012
K121487LITECURE THERAPY COMPACTJune 12, 2012
K103511LITECURE THERAPY SYSTEMJanuary 25, 2011
K093087BWF-5 MEDICAL LASER SERIESMay 12, 2010
K070400LC THERAPY, MODEL LCT-1000February 28, 2007