Bright Temporary C&B

Crown And Bridge, Temporary, Resin

DMP Dental Industry S.A.

The following data is part of a premarket notification filed by Dmp Dental Industry S.a. with the FDA for Bright Temporary C&b.

Pre-market Notification Details

Device IDK192830
510k NumberK192830
Device Name:Bright Temporary C&B
ClassificationCrown And Bridge, Temporary, Resin
Applicant DMP Dental Industry S.A. Kalyvion Avenue Markopoulo,  GR 19003
ContactDimitris Prantsidis
CorrespondentDimitris Prantsidis
DMP Dental Industry S.A. Kalyvion Avenue Markopoulo,  GR 19003
Product CodeEBG  
CFR Regulation Number872.3770 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2019-10-02
Decision Date2020-09-02

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
05206569722031 K192830 000
05206569001853 K192830 000
05206569001846 K192830 000
05206569001839 K192830 000
05206569001792 K192830 000
05206569001785 K192830 000
05206569001778 K192830 000
05206569001761 K192830 000
05206569001754 K192830 000
05206569001860 K192830 000
05206569001877 K192830 000
05206569722024 K192830 000
05206569721034 K192830 000
05206569721027 K192830 000
05206569001921 K192830 000
05206569001914 K192830 000
05206569001907 K192830 000
05206569001891 K192830 000
05206569001884 K192830 000
05206569001747 K192830 000

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