Product code EKY— Dental
DECIDENT
- Classification name
- Handpiece, Water-Powered
- Device class
- Class 1
- Regulation
- 21 CFR 872.4200
- Advisory panel
- Dental
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code EKY
FDA has cleared devices under product code EKY between 1990 and 2012, filed by 2 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
- 2012
- 1990
Top applicants under product code EKY
Recent clearances under product code EKY
Data sourced from openFDA. This site is unofficial and independent of the FDA.