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InMode Diolaze Device

Page Type
Cleared 510(K)
510(k) Number
K142952
510(k) Type
Traditional
Applicant
INMODE MD LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/13/2015
Days to Decision
95 days
Submission Type
Summary

InMode Diolaze Device

Page Type
Cleared 510(K)
510(k) Number
K142952
510(k) Type
Traditional
Applicant
INMODE MD LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/13/2015
Days to Decision
95 days
Submission Type
Summary