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iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183200
510(k) Type
Traditional
Applicant
C&E GP Specialist, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2019
Days to Decision
51 days
Submission Type
Summary

iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183200
510(k) Type
Traditional
Applicant
C&E GP Specialist, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2019
Days to Decision
51 days
Submission Type
Summary