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FDA 510(k) Applications Submitted by John Ray
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961375
04/09/1996
DIA SCREEN 10 WAY REAGENT STRIPS
GENESIS LABS, INC.
K232233
07/27/2023
Invisalign System with Mandibular Advancement Featuring Occlusal Blocks
Align Technology, Inc.
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