DeviceClearance

Product code JES— Dental

DENTAL FLOSS HOLDER

Classification name
Floss, Dental
Device class
Class 1
Regulation
21 CFR 872.6390
Advisory panel
Dental
Total cleared
62
First cleared
Most recent

Market context for product code JES

FDA has cleared 62 devices under product code JES between 1976 and 2009, filed by 45 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 JES

Recent clearances under product code JES

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