510(k) Report

FDA applicant

Doseoptics, LLC

Lebanon, NH2 decisions2020–20210 recalls

FDA records 2 decisions for Doseoptics, LLC (Lebanon, NH) from 2020 to 2021: 2 510(k) clearances. All are in product code IYE (Accelerator, Linear, Medical). Its devices cite 2 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, radiology panel, where it files most

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

FDA decisions per year

1in 2021

2020: 12021: 1
2020high 1 (2020) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Doseoptics, LLC by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IYEAccelerator, Linear, Medical2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K200940BeamSiteDoseoptics, LLC · 20201cites it

What has FDA decided for it lately?

  • K212606BeamSiteDoseoptics, LLC · 2021
  • K200940BeamSiteDoseoptics, LLC · 2020

All 2 as Doseoptics, LLC →