FDA 510(k) Applications Submitted by ADEOR MEDICAL AG

FDA 510(k) Number Submission Date Device Name Applicant
K130755 03/19/2013 HICUT HIGHSPEED INSTRUMENT ADEOR MEDICAL AG
K191847 07/10/2019 Adeor Medical nxt Non-stick Bipolar Forceps, Adeor Medical nxt Single-Use Non-stick Bipolar Forceps Adeor Medical AG
K191479 06/04/2019 Velocity Alpha Highspeed Surgical Drill System adeor Medical AG


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