DeviceClearance

Product code EJL— Dental

DENTAL BURS

Classification name
Bur, Dental
Device class
Class 1
Regulation
21 CFR 872.3240
Advisory panel
Dental
Total cleared
27
First cleared
Most recent

Market context for product code EJL

FDA has cleared 27 devices under product code EJL between 1976 and 2008, filed by 25 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 EJL

Adverse events under product code EJL

product code EJL
Other
1
Total
1

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 EJL

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