Product code DZS— Dental

FDA has cleared 4 devices under product code DZS between 1978 and 1982, 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.

• 19821 clearance
• 19801 clearance
• 19782 clearances

• Lee Pharmaceuticals2 clearances
• Syntex Dental Products, Inc.1 clearance
• Johnson & Johnson Professionals, Inc.1 clearance

• K822610 — PRECAPSULED DENTAL AMALGAMSyntex Dental Products, Inc.·1982-09-14
• K802967 — DISPERSALLOY-DISPERSED PHASE ALLOY SELF-Johnson & Johnson Professionals, Inc.·1980-12-30
• K781243 — MERCURY DISP. CAPSULELee Pharmaceuticals·1978-09-20
• K780966 — LEE-ALLOY DISPOSABLE CAPSULESLee Pharmaceuticals·1978-08-21