DeviceClearance

Product code JEQ— Dental

INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

Classification name
Toothbrush, Powered
Device class
Class 1
Regulation
21 CFR 872.6865
Advisory panel
Dental
Total cleared
54
First cleared
Most recent

Market context for product code JEQ

FDA has cleared 54 devices under product code JEQ between 1977 and 2020, filed by 48 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

last 15 years

Top applicants under product code JEQ

Adverse events under product code JEQ

product code JEQ
Injury
188
Malfunction
2,818
Total
3,006

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code JEQ

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