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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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