DeviceClearance

Product code EKX— Dental

Endo Motor

Classification name
Handpiece, Direct Drive, Ac-Powered
Device class
Class 1
Regulation
21 CFR 872.4200
Advisory panel
Dental
Total cleared
90
First cleared
Most recent

Market context for product code EKX

FDA has cleared 90 devices under product code EKX between 1976 and 2026, filed by 58 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 EKX

Recent clearances under product code EKX

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