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ARTIFICIAL TEETH, PORCELAIN, MODIFIED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860608
510(k) Type
Traditional
Applicant
DENTSPLY INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/1986
Days to Decision
35 days

ARTIFICIAL TEETH, PORCELAIN, MODIFIED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860608
510(k) Type
Traditional
Applicant
DENTSPLY INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/1986
Days to Decision
35 days