Product code EIB— Dental

FDA has cleared 4 devices under product code EIB between 1976 and 1991, filed by 4 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.

• 19911 clearance
• 19881 clearance
• 19831 clearance
• 19761 clearance

• Xomed, Inc.1 clearance
• Western Advanced Technology, Inc.1 clearance
• Cp Medical1 clearance
• Allergan, Inc.1 clearance

• K911118 — DTF-1000LL,DTF-1000Cp Medical·1991-11-20
• K874543 — MODEL OPO-32 IRRIGATION SLEEVEAllergan, Inc.·1988-01-14
• K822411 — SYSTEM 80 FACEPLATE-IN-THE-EAR #F1Western Advanced Technology, Inc.·1983-07-12
• K760570 — ROBINSON MIDDLE EAR PROSTHESISXomed, Inc.·1976-09-21