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Carl Zeiss Meditec Cataract Technologies

FDA Regulatory Profile

Carl Zeiss Meditec Cataract Technologies has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest 510(k)
Oct 15, 2026

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances1Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K262097MICOR 700 System (N/A); MICOR 700 Extractor (FG-50621)Oct 15, 2026

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.