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Refractec, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K053475
OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-450
March 3, 2006
K980522
REFRACTEC MCS-100
July 22, 1998