Product code EEF— Dental

FDA has cleared 3 devices under product code EEF between 1978 and 2007, filed by 3 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.

• 20071 clearance
• 19921 clearance
• 19781 clearance

• Sybron Dental Specialties, Inc.1 clearance
• Hygienic Dental Mfg., Co., The1 clearance
• Bay Technical Products, Inc.1 clearance

• K071615 — FIXAFLOSSSybron Dental Specialties, Inc.·2007-09-21
• K915207 — DISPOSABLE RADIOLUCENT RUBBER DAM CLAMPBay Technical Products, Inc.·1992-02-14
• K780744 — BRINKER TISSUE RETRACTORSHygienic Dental Mfg., Co., The·1978-05-12