Product code KLC— Dental

DENTAL CHAIR

Classification name
Chair, Dental, With Operative Unit
Device class
Class 1
Regulation
21 CFR 872.6250
Advisory panel
Dental
Total cleared
63
First cleared
Most recent

Market context for product code KLC

FDA has cleared 63 devices under product code KLC between 1976 and 2024, filed by 31 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 KLC

Recent clearances under product code KLC

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