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MODIFICATION TO RELIADENT DENTAL IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K061323
510(k) Type
Traditional
Applicant
BIOINFERA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2007
Days to Decision
377 days
Submission Type
Summary

MODIFICATION TO RELIADENT DENTAL IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K061323
510(k) Type
Traditional
Applicant
BIOINFERA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2007
Days to Decision
377 days
Submission Type
Summary