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

Adhese 2

K Number: K252450 · Decision Mar 5, 2026
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
65
Review Days
213

Basic Information

Device Name
Adhese 2
K Number
K252450
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivoclar Vivadent, Inc.
Date Received
August 4, 2025
Decision Date
March 5, 2026
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

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