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Imd, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K113662FENESTRATED NERVE BLOCK NEEDLEApril 20, 2012
K865082PROPHY CARE SOLUTIONFebruary 12, 1987
K864215PROPHY CARE SOLUTIONNovember 18, 1986
K863133PROPHY CARE PASTESeptember 25, 1986