Last synced on 25 January 2026 at 3:41 am

AURECAST SUPER INLAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001478
510(k) Type
Traditional
Applicant
Aurex SA (Pty) , Ltd.
Country
South Africa
FDA Decision
Substantially Equivalent
Decision Date
6/20/2000
Days to Decision
40 days
Submission Type
Summary

AURECAST SUPER INLAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001478
510(k) Type
Traditional
Applicant
Aurex SA (Pty) , Ltd.
Country
South Africa
FDA Decision
Substantially Equivalent
Decision Date
6/20/2000
Days to Decision
40 days
Submission Type
Summary