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

Dia-X Sil Bite

K Number: K254112 · Decision Mar 19, 2026
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
21
Review Days
90

Basic Information

Device Name
Dia-X Sil Bite
K Number
K254112
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DiaDent Group International
Date Received
December 19, 2025
Decision Date
March 19, 2026
Product Code
ELW
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
ELW Material, Impression

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