Epilog Laser Corp.

FDA Regulatory Profile

Epilog Laser Corp. appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0524-2025, Class II) was initiated on August 8, 2024.

Summary

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

Recent Recalls

NumberClassProductDate
Z-0524-2025Class IIFusion Pro 24, Model 17000August 8, 2024