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

Venus Diamond; Venus Diamond Flow; Venus Pearl; Venus Bulk Flow One

K Number: K260783 · Decision Mar 11, 2026
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
7
Review Days
1

Basic Information

Device Name
Venus Diamond; Venus Diamond Flow; Venus Pearl; Venus Bulk Flow One
K Number
K260783
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kulzer, LLC
Date Received
March 10, 2026
Decision Date
March 11, 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

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K Number Device Name
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K243910 Retraxil
K240660 Signum composite flow; Signum universal bond; Signum metal bond ; Signum composite; Signum matrix; Signum liquid; Signum cre-active
K233868 dima Print Teeth & Temp
K230644 Signum opaque F
K220605 Venus Bulk Flow ONE