China Daheng Group Inc.

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1145-2014Class IIDenlase: Diode Laser Therapy System and Penlase: Dental Laser Therapy System surgical powered. July 15, 2013

Recent 510(k) Clearances

K-NumberDeviceDate
K113212DENTAL LASER THERAPY SYSTEMNovember 16, 2011
K102669DIODE LASER THERAPY SYSTEMNovember 17, 2010