JEQ

INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

Advisory panel
Dental
Total cleared
54

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.