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Anodyne

FDA Regulatory Profile

Anodyne 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 May 13, 2016.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K160710Oasis Lacrimal Intubation SetMay 13, 2016
K902141ANOLIFT - PORTABLE & ANOLIFT - GANTRYSeptember 12, 1990

FDA data resources