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CREOKORREKT Aligners

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211427
510(k) Type
Traditional
Applicant
Creodent Prosthetics, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2022
Days to Decision
524 days
Submission Type
Summary

CREOKORREKT Aligners

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211427
510(k) Type
Traditional
Applicant
Creodent Prosthetics, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2022
Days to Decision
524 days
Submission Type
Summary