DeviceClearance

Product code EJF— Dental

MEMORY WIRE

Classification name
Bracket, Metal, Orthodontic
Device class
Class 1
Regulation
21 CFR 872.5410
Advisory panel
Dental
Total cleared
103
First cleared
Most recent

Market context for product code EJF

FDA has cleared 103 devices under product code EJF between 1977 and 2000, filed by 46 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 EJF

Recent clearances under product code EJF

1–100 of 103

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