Product code EAY— Dental
DEN-MAT FIBER OPTIC HALOGEN LIGHT
- Classification name
- Light, Fiber Optic, Dental
- Device class
- Class 1
- Regulation
- 21 CFR 872.4620
- Advisory panel
- Dental
- Total cleared
- 18
- First cleared
- Most recent
Market context for product code EAY
FDA has cleared devices under product code EAY between 1976 and 1995, filed by 12 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
- 1995
- 1994
- 1987
- 1983
- 1982
- 1981
- 1980
- 1979
- 1978
- 1977
- 1976
Top applicants under product code EAY
Recent clearances under product code EAY
- K953191 — MODEL A15-101
- K953192 — MODEL A15-103
- K935718 — JEDENTAL VLC DENTAL CURING LIGHT
- K871816 — STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TM
- K831976 — POWER OPTIC
- K831824 — DENTAL ELECTRONIC/S.B.R TRADING BU HAND
- K820907 — DENTISCOPE
- K812605 — FIBER OPTIC LIGHT SOURCE I
- K802684 — HELIOMAT
- K802716 — DEN-MAT FIBER OPTIC HALOGEN LIGHT
- K801591 — FIBER OPTIC ILLUMINATOR
- K801592 — FIBER OPTIC HOSE
- K791771 — ORALUMINATOR III AUTO-LIGHT
- K791733 — LIGHT-PAK
- K781878 — LIGHT, INSIDE
- K761331 — OPUS I OPTION - FIBER OPTIC L SYSTEM
- K760795 — FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C.
- K760796 — ORALUMINATOR III - LIGHT SOURCE FOR F.O.
Data sourced from openFDA. This site is unofficial and independent of the FDA.