Product code DYN— Dental

SALIVA EJECTOR

Classification name
Mouthpiece, Saliva Ejector
Device class
Class 1
Regulation
21 CFR 872.6640
Advisory panel
Dental
Total cleared
18
First cleared
Most recent

Market context for product code DYN

FDA has cleared 18 devices under product code DYN between 1976 and 1994, 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 DYN

Recent clearances under product code DYN

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