Product code KJJ— Unknown

FILE-EZE

Classification name
Cleanser, Root Canal
Device class
Unclassified
Advisory panel
Unknown
Total cleared
41
First cleared
Most recent

Market context for product code KJJ

FDA has cleared 41 devices under product code KJJ between 1978 and 2025, filed by 26 applicant companies. No FDA device recalls reference this product code.

Clearances per year

last 15 years

Top applicants under product code KJJ

Recent clearances under product code KJJ

Data sourced from openFDA. This site is unofficial and independent of the FDA.