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NEODENT IMPLANT SYSTEM, TITAMAX TI EX ACQUA AND TI DRIVE ACQUA, TITAMAX SMART EX ACQUA AND DRIVE SMART ACQUA, TITAMAX CM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133592
510(k) Type
Traditional
Applicant
NEODENT USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2014
Days to Decision
273 days
Submission Type
Summary

NEODENT IMPLANT SYSTEM, TITAMAX TI EX ACQUA AND TI DRIVE ACQUA, TITAMAX SMART EX ACQUA AND DRIVE SMART ACQUA, TITAMAX CM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133592
510(k) Type
Traditional
Applicant
NEODENT USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2014
Days to Decision
273 days
Submission Type
Summary