Fiagon GmbH

Fiagon GmbH holds 16 FDA 510(k) medical device clearances, first cleared 2014, most recent 2026.

Top product codes for Fiagon GmbH

Recent clearances by Fiagon GmbH

K261540 — Cube 4D Navigation System, VirtuEye ProCode PGW·2026-06-02
K230700 — RIWOtrack Navigation SystemCode OLO·2023-11-20
K230065 — VenSure Balloon Dilation System, VenSure Light Balloon Dilation System, VenSure Nav Balloon Dilation System, VenSure ET Balloon Dilation SystemCode PNZ·2023-05-26
K211291 — Cube Navigation System, VirtuEye V2, Navigation Sensor NanoRest, Navigation Unit Cube 4DCode PGW·2021-07-19
K201472 — VenSure Balloon Device, VenSure Nav Balloon DeviceCode LRC·2020-08-26
K200041 — FlexPointer 1.5 Single Use, FlexTube 3 Single UseCode PGW·2020-03-10
K163209 — Fiagon Navigation SystemCode HAW·2017-09-14
K163416 — Fiagon Navigation PointerTube Straight and PointerTube KeatCode PGW·2017-02-16
K162176 — Fiagon Navigation SystemCode PGW·2016-12-01
K161940 — Guidewire 0.6 Single UseCode PGW·2016-09-18
K151156 — Fiagon Navigation SystemCode HAW·2016-04-01
K160479 — PointerShell Universal, PointerShell LSCode PGW·2016-03-23
K160369 — GuideWireCode PGW·2016-03-10
K150473 — FlexPointer 1.5 mmCode PGW·2015-04-16
K141456 — THE FIAGON NAVIGATION - EXTENDED INSTRUMENT SET ENT, REGISTRATIONPOINTER, VENTERAPOINTER, GUIDEWIRE, POINTERSHELLCode PGW·2014-10-08
K133573 — FIAGON NAVIGATION SYSTEMCode PGW·2014-04-30

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