FDA applicant

Flow-Fx, LLC

Mokena, IL4 decisions2014–20240 recalls

FDA records 4 decisions for Flow-Fx, LLC (Mokena, IL) from 2014 to 2024: 4 510(k) clearances. Most are in product codes HSB (Rod, Fixation, Intramedullary And Accessories) and HWC (Screw, Fixation, Bone). Its devices cite 11 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Flow-Fx, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2014high 1 (2014) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Flow-Fx, LLC by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Flow-Fx, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Flow-Fx”

FDA records each applicant name separately; these may or may not be the same firm.

Flow Laboratories, Inc. 58 Flow X-Ray Corp. 2 Flow Neuroscience AB 1 Flow Cytometry Standards Corp. 1

Flow-Fx, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Flow-Fx”