Product code MEF— Dental
JEJE TEETHER
- Classification name
- Ring, Teething, Non-Fluid Filled
- Device class
- Class 1
- Regulation
- 21 CFR 872.5550
- Advisory panel
- Dental
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code MEF
FDA has cleared device under product code MEF, all in 2004, filed by 1 applicant company. 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.
Top applicants under product code MEF
Recent clearances under product code MEF
Data sourced from openFDA. This site is unofficial and independent of the FDA.