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FDA 510(k) Applications Submitted by DXM CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040116
01/20/2004
HAWK INTRAORAL CAMERA AND ACCESSORIES
DXM CO., LTD.
K042703
09/30/2004
CYBIRD LED CURING LIGHT
DXM CO., LTD.
K121093
04/10/2012
D1 LED CURING LIGHT, SPEC 3, DENTRONIX LED 3000
DXM CO., LTD.
K081694
06/17/2008
DENJECTOR
DXM CO., LTD.
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