FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

D1 LED CURING LIGHT, SPEC 3, DENTRONIX LED 3000

K Number: K121093 · Decision Nov 27, 2012
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
6
Review Days
231

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
D1 LED CURING LIGHT, SPEC 3, DENTRONIX LED 3000
K Number
K121093
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dxm Co., Ltd.
Date Received
April 10, 2012
Decision Date
November 27, 2012
Product Code
EBZ
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EBZ Activator, Ultraviolet, For Polymerization

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EBZ), ordered by most recent decision date.

View all

Other Clearances by Dxm Co., Ltd.

K Number Device Name
K191221 Cybird LED Curing Light
K173876 Cybird LED Curing Light
K081694 DENJECTOR
K042703 CYBIRD LED CURING LIGHT
K040116 HAWK INTRAORAL CAMERA AND ACCESSORIES