Refractec, Inc.

FDA Regulatory Profile

Refractec, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 3, 2006.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K053475OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-450March 3, 2006
K980522REFRACTEC MCS-100July 22, 1998