Last synced on 25 January 2026 at 3:41 am

miCOR System Lens Fragmentation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222236
510(k) Type
Special
Applicant
Carl Zeiss Meditec Cataract Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2022
Days to Decision
29 days
Submission Type
Statement

miCOR System Lens Fragmentation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222236
510(k) Type
Special
Applicant
Carl Zeiss Meditec Cataract Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2022
Days to Decision
29 days
Submission Type
Statement