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GENESIS DIODE LASER

Page Type
Cleared 510(K)
510(k) Number
K062258
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2007
Days to Decision
229 days
Submission Type
Summary

GENESIS DIODE LASER

Page Type
Cleared 510(K)
510(k) Number
K062258
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2007
Days to Decision
229 days
Submission Type
Summary