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Renamel® Microhybrid ;Renamel® Flowable Microhybrid

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222435
510(k) Type
Traditional
Applicant
Cosmedent, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2022
Days to Decision
60 days
Submission Type
Statement

Renamel® Microhybrid ;Renamel® Flowable Microhybrid

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222435
510(k) Type
Traditional
Applicant
Cosmedent, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2022
Days to Decision
60 days
Submission Type
Statement