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FDA 510(k) Applications Submitted by Orthoscan, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K133174
10/17/2013
ORTHOSCAN FD MINI C-ARM
ORTHOSCAN, INC.
K051754
06/29/2005
ORTHOSCAN, ORTHOSCAN HD
ORTHOSCAN, INC.
K113708
12/16/2011
ORTHOSCAN MOBILE DI MINI C-ARM
ORTHOSCAN, INC.
K213113
09/27/2021
Orthoscan Tau Mini C-Arm
Orthoscan, Inc.
K183220
11/20/2018
OrthoScan TAU Mini C-Arm
Orthoscan, Inc.
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