Product code EIY— Dental

FDA has cleared 5 devices under product code EIY between 1982 and 1987, 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.

• 19871 clearance
• 19851 clearance
• 19841 clearance
• 19831 clearance
• 19821 clearance

• Dentsply Intl.2 clearances
• Miltex, Inc.1 clearance
• Artiberia1 clearance
• Almore Intl., Inc.1 clearance

• K871909 — COMPOSITE RESTORATIVE CARRIERDentsply Intl.·1987-05-27
• K851726 — 1760/1 TO 2010/34 VARIOUS DENTAL FILLING INSTRUMENArtiberia·1985-07-02
• K833955 — NOVEL DISPENSER/PACKAGEDentsply Intl.·1984-01-03
• K830776 — MICROFIL CONTOURING INSTRUMENTSAlmore Intl., Inc.·1983-04-28
• K823323 — DENTAL INSTRUMENTS - PLASTIC INSTRUMENTSMiltex, Inc.·1982-11-24