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

DENTAURUM GLASTEC DENTAL ORTHODONTIC CEMENT

K Number: K032195 · Decision Oct 7, 2003
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
7
Review Days
81

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Basic Information

Device Name
DENTAURUM GLASTEC DENTAL ORTHODONTIC CEMENT
K Number
K032195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3750
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dentaurum
Date Received
July 18, 2003
Decision Date
October 7, 2003
Product Code
DYH
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
DYH Adhesive, Bracket And Tooth Conditioner, Resin

Similar 510(k) Clearances

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

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Other Clearances by Dentaurum

K Number Device Name
K062733 TOMAS PIN SD 6, 8, AND 10 MM
K062732 TOMAS PIN 6 MM
K030644 CONTEC DUO, CONTEC LC, CONTEC LCR
K030980 DENTAURUM NO-MIX ONE STEP BRACKET ADHESIVE
K030977 DENTAURUM MIX TWO-PASTE BRACKET ADHESIVE
K030641 CONTEC LIGHT