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FDA 510(k) Applications Submitted by G & H WIRE CO.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081393
05/19/2008
ORTHODONTIC TEMPORARY ANCHORAGE IMPLANT SCREW
G & H WIRE CO.
K961754
05/06/1996
SAFETY RELEASE MODULE
G & H WIRE CO.
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