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Espe Dental Products

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K810950VISIO-SEALApril 29, 1981
K802819KETAC-CEM IN REF. TO K802048November 24, 1980
K802049NIMETIC-DISPERSSeptember 16, 1980
K800031PERMADYNE POLYETHER RUBBER IMPRESSIONFebruary 5, 1980
K771889UNIOLITEOctober 20, 1977
K771901CAPMIXOctober 20, 1977
K771120IMPREFLEX ALGINATE IMPRESSION MATERIALAugust 3, 1977
K771119PASTES, RESTORATIVE & TINTED, DEBTALJuly 15, 1977