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Dentronix, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K910202DENTRONIX MODEL 2000March 13, 1991
K880322DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEMJuly 13, 1988
K771006MODIFIED PODIATRY PRODUCTSJune 17, 1977
K771005NEW PODIATRY PRODUCTSJune 17, 1977
K770302CUTTER, P606 BONEMarch 9, 1977
K770303NIPPER, NAIL, P610 ENGLISHMarch 9, 1977
K770305CUTTER, P607 BONEMarch 9, 1977
K770304CUTTER, P605 GENERAL PURPOSEMarch 9, 1977
K770301NIPPER, PSO4 TISSUEMarch 7, 1977