Fiagon GmbH

15 FDA 510(k) medical device clearances.

Top product codes for Fiagon GmbH

Recent clearances by Fiagon GmbH

K230700 — RIWOtrack Navigation System OLO · 2023-11-20
K230065 — VenSure Balloon Dilation System, VenSure Light Balloon Dilation System, VenSure Nav Balloon Dilation System, VenSure ET Balloon Dilation System PNZ · 2023-05-26
K211291 — Cube Navigation System, VirtuEye V2, Navigation Sensor NanoRest, Navigation Unit Cube 4D PGW · 2021-07-19
K201472 — VenSure Balloon Device, VenSure Nav Balloon Device LRC · 2020-08-26
K200041 — FlexPointer 1.5 Single Use, FlexTube 3 Single Use PGW · 2020-03-10
K163209 — Fiagon Navigation System HAW · 2017-09-14
K163416 — Fiagon Navigation PointerTube Straight and PointerTube Keat PGW · 2017-02-16
K162176 — Fiagon Navigation System PGW · 2016-12-01
K161940 — Guidewire 0.6 Single Use PGW · 2016-09-18
K151156 — Fiagon Navigation System HAW · 2016-04-01
K160479 — PointerShell Universal, PointerShell LS PGW · 2016-03-23
K160369 — GuideWire PGW · 2016-03-10
K150473 — FlexPointer 1.5 mm PGW · 2015-04-16
K141456 — THE FIAGON NAVIGATION - EXTENDED INSTRUMENT SET ENT, REGISTRATIONPOINTER, VENTERAPOINTER, GUIDEWIRE, POINTERSHELL PGW · 2014-10-08
K133573 — FIAGON NAVIGATION SYSTEM PGW · 2014-04-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.