FDA applicant

Sibel, Inc.

Niles, IL3 decisions2021–20220 recalls

FDA records 3 decisions for Sibel, Inc. (Niles, IL) from 2021 to 2022: 3 510(k) clearances. Most are in product codes DRG (Transmitters And Receivers, Physiological…) and MNR (Ventilatory Effort Recorder). Its devices cite 3 predicates, 1 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, cardiovascular panel, where it files most

How often FDA has decided Sibel, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2022

2021high 2 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Sibel, Inc. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sibel, Inc.’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 “Sibel”

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

Sibel Health, Inc. 5

Sibel, Inc.

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 “Sibel”