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Iridex TruFocus LIO Premiere

Page Type
Cleared 510(K)
510(k) Number
K181662
510(k) Type
Special
Applicant
Iridex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2018
Days to Decision
72 days
Submission Type
Summary

Iridex TruFocus LIO Premiere

Page Type
Cleared 510(K)
510(k) Number
K181662
510(k) Type
Special
Applicant
Iridex Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2018
Days to Decision
72 days
Submission Type
Summary