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Luma Vision Limited
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K260885
VERAFEYE Imaging and Guidance System (VF-VIS-002)
June 15, 2026
K242893
VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System
March 24, 2025