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NewVision SC (tisilfocon A) Scleral Lens; NewVision SC Daily Wear Ortho-K (tisilfocon A) Corneo-Scleral Lens

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230910
510(k) Type
Traditional
Applicant
Acculens, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2023
Days to Decision
77 days
Submission Type
Summary

NewVision SC (tisilfocon A) Scleral Lens; NewVision SC Daily Wear Ortho-K (tisilfocon A) Corneo-Scleral Lens

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230910
510(k) Type
Traditional
Applicant
Acculens, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2023
Days to Decision
77 days
Submission Type
Summary