Product code EIL— Dental

FDA has cleared 8 devices under product code EIL between 1982 and 1991, 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.

• 19911 clearance
• 19893 clearances
• 19881 clearance
• 19872 clearances
• 19821 clearance

• Abiomed, Inc.2 clearances
• Vine Valley Research1 clearance
• National Patent Development Corp.1 clearance
• Florida Probe Corp.1 clearance
• Dr. Bernard Loewenthal1 clearance
• Dentsply Intl.1 clearance
• Bowen & Company, Inc.1 clearance

• K911643 — ABIODENT PERIOTEMP(R) SYSTEMAbiomed, Inc.·1991-07-09
• K890493 — FLORIDA PROBE PERIODONTAL PROBEFlorida Probe Corp.·1989-03-13
• K885075 — ABIOMED PERIOTEMP(TM) PROBEAbiomed, Inc.·1989-02-13
• K884813 — MODEL 200A ELECTRONIC FORCE-SENSING PROBEVine Valley Research·1989-01-05
• K880209 — PERIODONTAL PROBE - AUTOPROBEDentsply Intl.·1988-04-27
• K872098 — CREMEEN ALVEOLAR BONE CALIPERBowen & Company, Inc.·1987-07-31
• K872215 — PERIO-TESTDr. Bernard Loewenthal·1987-07-10
• K822793 — PIO ROOT CANAL INDICATORNational Patent Development Corp.·1982-10-22