510(k) Report

FDA applicant

Best Industries

Springfield, VA9 decisions1991–19940 recalls

FDA records 9 decisions for Best Industries (Springfield, VA) from 1991 to 1994: 9 510(k) clearances. Most are in product codes IWJ (System, Applicator, Radionuclide, Manual) and KXK (Source, Brachytherapy, Radionuclide). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Best Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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