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

Dia-Cem

K Number: K231552 · Decision Jul 28, 2023
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
21
Review Days
59

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Dia-Cem
K Number
K231552
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DiaDent Group International
Date Received
May 30, 2023
Decision Date
July 28, 2023
Product Code
EMA
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
EMA Cement, Dental

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EMA), ordered by most recent decision date.

View all

Other Clearances by DiaDent Group International

K Number Device Name
K261093 DIAFIL
K261071 DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)
K254112 Dia-X Sil Bite
K220804 Dia-X Bond Universal
K213401 DIAPLUS Universal
K210421 Diafil & Diafil Capsule
K210333 DiaPaste
K200174 DIA-ROOT BIO MTA
K200809 D-LUX+
K200175 DIA-ROOT BIO Sealer
Search all 21 clearances from DiaDent Group International →