Product code EIX— Dental

FDA has cleared 9 devices under product code EIX between 1982 and 1996, filed by 9 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.

• 19961 clearance
• 19942 clearances
• 19891 clearance
• 19882 clearances
• 19872 clearances
• 19821 clearance

• Sweet Micro Systems, Inc.1 clearance
• Rms Div.1 clearance
• Pro-Dentec1 clearance
• Periodontal Health Brush, Inc.1 clearance
• Pd International AB1 clearance
• Miltex, Inc.1 clearance
• Florida Probe Corp.1 clearance
• Alpkem Corp.1 clearance
• Accudent, Inc.1 clearance

• K960245 — VIP VICTOR INTERACTIVE PROBEPro-Dentec·1996-04-04
• K944848 — THE VIVACARE T.P.S. PROBERms Div.·1994-12-14
• K936221 — PROBE TIP/PERI PROBE/PERI PROBE COMP.Pd International AB·1994-08-01
• K890333 — ALBUMIN REAGENTAlpkem Corp.·1989-02-17
• K880827 — ACCUTEK PERIODONTAL PROBESweet Micro Systems, Inc.·1988-04-12
• K875076 — FLORIDA PROBEFlorida Probe Corp.·1988-03-10
• K870280 — ACCUDENT ACCUPROBEAccudent, Inc.·1987-06-08
• K871504 — DISPOSABLE PERIODONTAL PROBEPeriodontal Health Brush, Inc.·1987-05-06
• K823324 — DENTAL INSTRUMENTS - PROBESMiltex, Inc.·1982-11-24