Product code EID— Dental

FDA has cleared 13 devices under product code EID between 1977 and 1994, filed by 10 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.

• 19941 clearance
• 19921 clearance
• 19872 clearances
• 19861 clearance
• 19852 clearances
• 19813 clearances
• 19781 clearance
• 19772 clearances

• Espe GmbH (Us)2 clearances
• Dentsply Intl.2 clearances
• Centrix, Inc.2 clearances
• Unitek Corp.1 clearance
• Lee Pharmaceuticals1 clearance
• G-C Intl. Corp.1 clearance
• Coltene, Inc.1 clearance
• Cavitron Corp.1 clearance
• Caulk Co., Div. Dentsply1 clearance
• Bio-Interfaces, Inc.1 clearance

• K941431 — BONE GRAFT DELIVERY SYRINGESBio-Interfaces, Inc.·1994-07-12
• K913974 — ACCESS IMPRESSION BARRELCentrix, Inc.·1992-02-25
• K873153 — CAULK'S VPS CARTRIDGE SYSTEMDentsply Intl.·1987-09-16
• K871937 — IMPRESSION SYRINGEDentsply Intl.·1987-06-05
• K863998 — COLTENE JET-MIXERColtene, Inc.·1986-10-30
• K853282 — CENTRIX RIBBON TUBESCentrix, Inc.·1985-08-23
• K851386 — UNITEK DISPOSABLE IMPRESSION SYRINGEUnitek Corp.·1985-04-29
• K812680 — G-C IMPRESSION SYRINGEG-C Intl. Corp.·1981-10-06
• K812277 — PRISMA-FIL COMPULESCaulk Co., Div. Dentsply·1981-09-08
• K811582 — THE PLACERCavitron Corp.·1981-07-28
• K781977 — APPLICATOR, LEE IMPRESSIONLee Pharmaceuticals·1978-12-20
• K770931 — APPLIC SYSTEM APPLIER, ESPEEspe GmbH (Us)·1977-06-03
• K770941 — APPLIC SYSTEM ACTIVATOR, ESPEEspe GmbH (Us)·1977-06-02