FDA 510(k) Applications Submitted by Remex Medical Corp.

FDA 510(k) Number Submission Date Device Name Applicant
K251315 04/29/2025 Anatase Spine Surgery Navigation System and Remex Spine Surgery Navigation System II Remex Medical Corp.
K243560 11/18/2024 Remex Spine Surgery Navigation Instrument Remex Medical Corp.
K230783 03/22/2023 Anatase Spine Surgery Navigation System Remex Medical Corp.
K241625 06/06/2024 Anatase Navi Disposable Instrument Remex Medical Corp.
K233513 11/01/2023 Remex Spine Surgery Navigation System II Remex Medical Corp.


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