FDA applicant

Proxima Therapeutics, Inc.

Alpharetta, GA5 decisions2001–20040 recalls

FDA records 5 decisions for Proxima Therapeutics, Inc. (Alpharetta, GA) from 2001 to 2004: 5 510(k) clearances. Most are in product codes JAQ (System, Applicator, Radionuclide…) and KXK (Source, Brachytherapy, Radionuclide). Its devices cite 13 predicates, 6 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 Proxima Therapeutics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Proxima Therapeutics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Proxima Therapeutics, 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?