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

IPS e.max Zirconia

K Number: K253953 · Decision Mar 10, 2026
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
65
Review Days
90

Basic Information

Device Name
IPS e.max Zirconia
K Number
K253953
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivoclar Vivadent, Inc.
Date Received
December 10, 2025
Decision Date
March 10, 2026
Product Code
EIH
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
EIH Powder, Porcelain

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