Aura Lens Products

FDA Regulatory Profile

Aura Lens Products appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 27, 1987.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K872506MELANITE IJuly 27, 1987
K852403AURALITE IIAugust 20, 1985