Product code KXR— Dental

BRUSH, APPLICATOR

Classification name: Applicator, Resin
Device class: Class 1
Regulation: 21 CFR 872.3140
Advisory panel: Dental
Total cleared: 3
First cleared: 1977-01-31
Most recent: 1983-10-04

Market context for product code KXR

FDA has cleared 3 devices under product code KXR between 1977 and 1983, filed by 3 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

19831 clearance
19781 clearance
19771 clearance

Top applicants under product code KXR

Deringer-Ney, Inc.1 clearance
Centrix, Inc.1 clearance
3M Company1 clearance

Recent clearances under product code KXR

K832662 — DENTAL SYRINGE SYSTEM-VARIOUS STYLESCentrix, Inc.·1983-10-04
K781098 — BRUSH, APPLICATOR3M Company·1978-09-29
K770160 — CERAMIST BRUSHDeringer-Ney, Inc.·1977-01-31

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