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Moria SA

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K172994EPI K ConsoleOctober 26, 2017
K043183EPI-KMarch 25, 2005
K032836M3 MICROKERATOMEJune 18, 2004
K040297ONEUSE- PLUS MICROKERATOMEMarch 31, 2004
K022560M2 SINGLE USE MICROKERTOMESeptember 27, 2002
K003594CARRIAZO BARRAQUER SINGLE USE MICROKERATOMEMarch 9, 2001
K002191CARRIAZO BARRAQUER II MICROKERATOMEOctober 12, 2000
K981742ONE UP DISPOSABLE KERATOME HEADAugust 25, 1998
K981741CARRIAZO BARRAQUER MICROKERATOMEJuly 24, 1998