Product code EAZ— Dental
DENTAL LIGHT
- Classification name
- Light, Operating, Dental
- Device class
- Class 1
- Regulation
- 21 CFR 872.4630
- Advisory panel
- Dental
- Total cleared
- 23
- First cleared
- Most recent
Market context for product code EAZ
FDA has cleared devices under product code EAZ between 1976 and 2007, filed by 21 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.
Clearances per year
last 15 years- 2007
- 2005
- 2004
- 2001
- 1994
- 1993
- 1992
- 1991
- 1990
- 1989
- 1988
- 1986
- 1984
- 1980
- 1979
Top applicants under product code EAZ
Recent clearances under product code EAZ
- K072309 — MICROLUX/BLU
- K041614 — MICROLUX DL
- K033033 — VIZILITE-BLUE ORAL EXAM KIT
- K003995 — SPECULITE/ORALLITE
- K926081 — DENTAL LIGHT
- K935390 — SIROLUX FANTASTIC
- K925629 — ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT
- K923462 — DELIGHT
- K912142 — MICRONAIRE ISO-HOOD MAX 5UV
- K912997 — MINIFLEX AND PERSONAL UNIT
- K902685 — DEFIANCE MODEL FUS 336
- K894059 — ISOLIGHT
- K893044 — A-DEC DENTAL LIGHT
- K891216 — DENTAL EQUIPMENT PROTECTION DEVICES
- K884223 — DENTAL LAMP HANDLE COVER
- K874374 — THE WOOG ORATEST
- K863019 — F-11 REFLECTOR / F-II STANDARD REFLECTOR
- K832919 — OPTI-BEAM IV
- K801683 — LUNA-VUE DENTAL OPERATING LIGHT
- K790984 — KLIP-LITE
- K772351 — DENTAL LIGHT
- K771249 — JOY LIGHT
- K760707 — RITTER STARLIGHT DENTAL OPERATING LIGHT
Data sourced from openFDA. This site is unofficial and independent of the FDA.