FDA applicant

Alton Design, LLC

Singer Island, FL1 decision2003–20030 recalls

FDA records 1 decision for Alton Design, LLC (Singer Island, FL) in 2003: 1 510(k) clearance. All are in product code KXK (Source, Brachytherapy, Radionuclide). Its devices cite 9 predicates, 0 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, radiology panel, where it files most

How often FDA has decided Alton Design, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alton Design, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Alton Design, LLC’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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Other applicant names beginning “Alton”

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

Alton (Shanghai) Medical Instruments Co., Ltd. 6 Alton Dean Medical, Inc. 1

Alton Design, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Alton”