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Magentiq Eye, Ltd.

FDA Regulatory Profile

Magentiq Eye, Ltd. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 3, 2026

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances4Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K260724MAGENTIQ-COLO (ME-APDS)Apr 3, 2026
K252178MAGENTIQ-COLO (ME-APDS)Oct 3, 2025
K244023MAGENTIQ-COLO (ME-APDS)Jan 24, 2025
K223473ME-APDS™; MAGENTIQ-COLO™Jul 25, 2023

FDA data resources

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