FDA applicant

Beamline Corporation

Irvine, CA1 decision2005–20050 recalls

FDA records 1 decision for Beamline Corporation (Irvine, CA) in 2005: 1 510(k) clearance. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Beamline Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Beamline Corporation by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Beamline Corporation’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

Beamline Corporation

Which product codes does it file in?

What has FDA decided for it lately?