DeviceClearance

Product code KMT— Dental

DENTAL VACUUM INJECTION TRAY

Classification name
Tray, Fluoride, Disposable
Device class
Class 1
Regulation
21 CFR 872.6870
Advisory panel
Dental
Total cleared
8
First cleared
Most recent

Market context for product code KMT

FDA has cleared 8 devices under product code KMT between 1977 and 2004, filed by 8 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 KMT

Recent clearances under product code KMT

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