FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Grandio disc multicolor

K Number: K261357 · Decision Apr 27, 2026
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
119
Review Days
3

Basic Information

Device Name
Grandio disc multicolor
K Number
K261357
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Voco GmbH
Date Received
April 24, 2026
Decision Date
April 27, 2026
Product Code
EBF
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

Classifications

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

Product Code Device Name
EBF Material, Tooth Shade, Resin

Similar 510(k) Clearances

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

View all

Other Clearances by Voco GmbH

K Number Device Name
K252073 VOCO Profluorid Varnish + BioMin
K252606 Bifix Veneer LC, Bifix Veneer Try-In
K251390 MTA vpt
K251239 GrandioSO Unlimited
K231817 AlignerFlow LC
K231591 V-Print c&b temp
K230877 Admira Fusion 5
K220236 V-Print dentbase
K220640 Bifix Hybrid Abutment Cement
K220743 CediTEC
Search all 119 clearances from Voco GmbH →