Product code EJE— Dental

FDA has cleared 3 devices under product code EJE between 1977 and 1978, 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.

• 19782 clearances
• 19771 clearance

• Hygienic Dental Mfg., Co., The2 clearances
• Young Dental Manufacturing Co. 1, LLC1 clearance

• K781520 — RUBBER DAM HOLDERYoung Dental Manufacturing Co. 1, LLC·1978-10-10
• K780746 — HYGIENIC RUBBER DAM FRAMEHygienic Dental Mfg., Co., The·1978-05-12
• K770117 — HYGIENIC 5 & 6 RUBBER DAM FRAMEHygienic Dental Mfg., Co., The·1977-01-28