510(k) K253248

Device
Bright Cavity Liner
Applicant
Dmp Dental Industry S.A.
510(k) number
K253248
Product code
EJK
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-13
Date received
2025-09-29
Regulation
872.3250
Classification name
Liner, Cavity, Calcium Hydroxide
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Related Records

Applicant Contact

Contact
Konstantinos Kyritsis
Address
Kalyvion Ave. Markopoulo GR 19003 19003

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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