FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)

K Number: K261071 · Decision May 19, 2026
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
21
Review Days
48

Basic Information

Device Name
DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)
K Number
K261071
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DiaDent Group International
Date Received
April 1, 2026
Decision Date
May 19, 2026
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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Other Clearances by DiaDent Group International

K Number Device Name
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K210421 Diafil & Diafil Capsule
K210333 DiaPaste
K200174 DIA-ROOT BIO MTA
K200809 D-LUX+
K200175 DIA-ROOT BIO Sealer
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