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Restor3d Utility Wedge

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201314
510(k) Type
Traditional
Applicant
Restor3D, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2021
Days to Decision
395 days
Submission Type
Summary

Restor3d Utility Wedge

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201314
510(k) Type
Traditional
Applicant
Restor3D, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2021
Days to Decision
395 days
Submission Type
Summary