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Endomedics, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K831792SELF-ALIGNING ACETABULAR COMPONENTSeptember 20, 1984
K842234NEW JERSEY FEMORAL STEMJuly 20, 1984
K842233NEW JERSEY FEMORAL RESURFACING COMPONENTJuly 20, 1984
K842202NEW JERSEY ACETABULAR COMPONENT &July 20, 1984