Product code ELZ— Dental

FDA has cleared 9 devices under product code ELZ between 1977 and 2009, filed by 7 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.

• 20091 clearance
• 19941 clearance
• 19931 clearance
• 19912 clearances
• 19891 clearance
• 19881 clearance
• 19772 clearances

• George M. Wilson, Dds3 clearances
• Whitecap Dental Co.1 clearance
• Svenska Dental Instruments AB1 clearance
• Sterndent Corp.1 clearance
• South American Dental Exporting Corp.1 clearance
• Parker Laboratories, Inc.1 clearance
• Ez-Pedo, Inc.1 clearance

• K091362 — CERAMIC PEDATRIC PREFORMED CROWNEz-Pedo, Inc.·2009-06-29
• K932759 — TEMPOARY POLYCARBONATE CROWNSSouth American Dental Exporting Corp.·1994-07-22
• K931352 — PEDO JACKETS OR PJ'SGeorge M. Wilson, Dds·1993-07-21
• K913152 — WHITER BITER CROWNGeorge M. Wilson, Dds·1991-09-30
• K912686 — WHITER BITER CROWNGeorge M. Wilson, Dds·1991-09-16
• K892893 — SDI POLYCARBONATE CROWN, SCHEIN'SSvenska Dental Instruments AB·1989-06-06
• K883325 — PERFORMED CROWN (STAINLESS STEEL)Whitecap Dental Co.·1988-09-16
• K771128 — NEKO CERAMIC CONVENIENCE CROWNSSterndent Corp.·1977-07-15
• K770684 — CROWN, ACRYLIC, CORAL BRAND, PREFORMEDParker Laboratories, Inc.·1977-04-26