FDA 510(k) Applications Submitted by Disior Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K240736 03/18/2024 SMART Bun-Yo-Matic X-Ray Disior Ltd
K240642 03/06/2024 SMART Bun-Yo-Matic CT Disior Ltd
K223757 12/15/2022 Bonelogic Disior Ltd
K203290 11/09/2020 Bonelogic Disior Ltd


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