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Nexmed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K033580NEXFLEX TOTAL HIP SYSTEMAugust 5, 2004
K991882NEXFLEX TOTAL KNEE SYSTEMDecember 8, 1999
K955170NEXFLEX FEMORAL STEM, STANDARD DESIGNFebruary 9, 1996
K955171NEXLOCK FEMORAL STEMFebruary 9, 1996
K952629NEXFLEX TOTAL HIP SYSTEMSeptember 8, 1995
K951656NEXMED CANCELLOUS BONE SCREWSJuly 18, 1995