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Locator Overdenture Implant System

Page Type
Cleared 510(K)
510(k) Number
K203701
510(k) Type
Traditional
Applicant
Ivory Super Holdco Inc. / Zest Anchors LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2021
Days to Decision
118 days
Submission Type
Summary

Locator Overdenture Implant System

Page Type
Cleared 510(K)
510(k) Number
K203701
510(k) Type
Traditional
Applicant
Ivory Super Holdco Inc. / Zest Anchors LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2021
Days to Decision
118 days
Submission Type
Summary