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Almore Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K862851ALMORE FACE MASKAugust 12, 1986
K854692MONARCH II BLEACHING INSTRUMENTMay 12, 1986
K854696OP II VISIBLE LIGHT CURING SYSTEMMarch 26, 1986
K854690DIAMONDS BURS-COMPOSIT FINISHINGMarch 25, 1986
K854691DIAMOND BURS-HANDPIECEMarch 25, 1986
K854700EZ-ON TUBING CONDITIONER (LUBRICANT)March 12, 1986
K854702PLASTIC MOUNTING RINGSMarch 6, 1986
K854701RETRACT-A-CORDMarch 6, 1986
K854697TUBING HANDPIECE REPLACEMENTMarch 6, 1986
K854699TUBING SYRINGJanuary 6, 1986
K831136DOUBLE BOW TOOTH SEPARATORJune 8, 1983
K831137STRAIGHT 5 HEMOSTATMay 18, 1983
K831138CURVED HEMOSTAT 5May 18, 1983
K830776MICROFIL CONTOURING INSTRUMENTSApril 28, 1983
K830773MARKLEY THREADED WIREApril 28, 1983
K830775FACEBOW FOR BALANCE ARTICULATORApril 28, 1983
K830774BINOCULAR MAGNIFIER 2XApril 6, 1983
K830878BINOCULAR LOUPEApril 6, 1983
K830777ELECTRIC MOUTH MIRRORApril 6, 1983
K811075BALANCE ARTICULATORMay 13, 1981