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FDA 510(k) Applications Submitted by ROBERT YAMASHITA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K092743
09/08/2009
THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM
STRYKER CRANIOMAXILLOFACIAL
K233098
09/26/2023
MYOTouch Muscle Stimulator
SunMed LLC.
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