510(k) K172407

Device
Duracetal
Applicant
The Myerson Company Limited
510(k) number
K172407
Product code
EBI  
Decision
Substantially Equivalent (SESE)
Decision date
2017-11-02
Date received
2017-08-09
Regulation
872.3760
Classification name
Resin, Denture, Relining, Repairing, Rebasing
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Cindy Buchoon-Legendre
Address
3 Trinity Ave. Laventille TT

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00304040151549ZirluxHENRY SCHEIN, INC.2021-03-11
00304040151532ZirluxHENRY SCHEIN, INC.2021-03-11
00304040151525ZirluxHENRY SCHEIN, INC.2021-03-11
00304040151518ZirluxHENRY SCHEIN, INC.2021-03-11
00304040151501ZirluxHENRY SCHEIN, INC.2021-03-11
00304040151495ZirluxHENRY SCHEIN, INC.2021-03-11
00842326104389DuracetalThe Myerson Company Limited2020-09-25
00842326104372DuracetalThe Myerson Company Limited2020-09-25
00842326104365DuracetalThe Myerson Company Limited2020-09-25
00842326104358DuracetalThe Myerson Company Limited2020-09-25
00842326104341DuracetalThe Myerson Company Limited2020-09-25
00842326104228DuracetalThe Myerson Company Limited2020-09-25

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K242897Partial FlexClemde SA DE CV2025-06-03
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Legacy Summary

summary

FDA Review

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