DeviceClearance

Product code EFA— Dental

ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE

Classification name
Handpiece, Belt And/Or Gear Driven, Dental
Device class
Class 1
Regulation
21 CFR 872.4200
Advisory panel
Dental
Total cleared
25
First cleared
Most recent

Market context for product code EFA

FDA has cleared 25 devices under product code EFA between 1980 and 2020, filed by 18 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

Top applicants under product code EFA

Recent clearances under product code EFA

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