Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Fiagon GmbH — Predicate Candidate Screening

16 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

84 daysmedian FDA review time
303 days90th percentile
16clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K261540Cube 4D Navigation System, VirtuEye ProFiagon GmbH2026-06-02250
K230700RIWOtrack Navigation SystemFiagon GmbH2023-11-202520
K230065VenSure™ Balloon Dilation System, VenSure™ Light Balloon DilFiagon GmbH2023-05-261370
K211291Cube Navigation System, VirtuEye V2, Navigation Sensor NanoRFiagon GmbH2021-07-19820
K201472VenSure Balloon Device, VenSure Nav Balloon DeviceFiagon GmbH2020-08-26840
K200041FlexPointer 1.5 Single Use, FlexTube 3 Single UseFiagon GmbH2020-03-10620
K163209Fiagon Navigation SystemFiagon GmbH2017-09-143030
K163416Fiagon Navigation – PointerTube Straight and PointerTube KeaFiagon GmbH2017-02-16730
K162176Fiagon Navigation SystemFiagon GmbH2016-12-011200
K161940Guidewire 0.6 Single UseFiagon GmbH2016-09-18660
K151156Fiagon Navigation SystemFiagon GmbH2016-04-013360
K160479PointerShell Universal, PointerShell LSFiagon GmbH2016-03-23300
K160369GuideWireFiagon GmbH2016-03-10290
K150473FlexPointer 1.5 mmFiagon GmbH2015-04-16520
K141456THE FIAGON NAVIGATION - EXTENDED INSTRUMENT SET ENT, REGISTRFiagon GmbH2014-10-081280
K133573FIAGON NAVIGATION SYSTEMFiagon GmbH2014-04-301610

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda