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MODIFICATION TO 3I PATIENT-SPECIFIC DENTAL ABUTMENTS AND OVERDENTURE BARS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052648
510(k) Type
Special
Applicant
Implant Innovations, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2005
Days to Decision
24 days
Submission Type
Summary

MODIFICATION TO 3I PATIENT-SPECIFIC DENTAL ABUTMENTS AND OVERDENTURE BARS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052648
510(k) Type
Special
Applicant
Implant Innovations, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2005
Days to Decision
24 days
Submission Type
Summary