Last synced on 25 January 2026 at 3:41 am

KDF Zirconia Disc

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221429
510(k) Type
Traditional
Applicant
Denken-Highdental Co., Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/14/2022
Days to Decision
59 days
Submission Type
Summary

KDF Zirconia Disc

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221429
510(k) Type
Traditional
Applicant
Denken-Highdental Co., Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/14/2022
Days to Decision
59 days
Submission Type
Summary