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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